(Q34691482)

4 August 2017

1 reference

title

The Cri du Chat syndrome: epidemiology, cytogenetics, and clinical features (English)

1 reference

4 August 2017

1 reference

Niebuhr E

1

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4 August 2017

publication date

1 November 1978

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4 August 2017

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4 August 2017

volume

44

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4 August 2017

issue

3

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4 August 2017

page(s)

227-275

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4 August 2017

cites work

The cri du chat syndrome

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Microcephaly, mental retardation and hypertelorism in chromosome deletion studies

21 January 2018

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Segregation of a balanced translocation t(5p-;Gp+)

21 January 2018

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12 December 2020

Mental retardation with 45 chromosomes 45,XX,--5,--14,+der(5) t(5,14)(p15;q13) mat due to familial balanced reciprocal translocation

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12 December 2020

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12 December 2020

Points of exchange in a human no. 5 ring chromosome

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https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

https://pubmed.ncbi.nlm.nih.gov/365706

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12 December 2020

[A case of deletion of the short arm of chromosome 5 in Vietnam (crying cat syndrome)]

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https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Structural variation in human nitotic chromosomes

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https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Measurements on hand radiographs from 32 cri-du-chat probands

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Crying cat syndrome discovered during a routine examination

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Modifications of cutaneous elastic fibers in cyring cat disease (apropos of a further case)

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Crying cat syndrome. Report of a case

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

THE "CAT CRY" SYNDROME.

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Crying cat syndrome with translocation 5/D 2

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

A deleted B chromosome in a mosaic mother and her cri du chat progeny

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

https://pubmed.ncbi.nlm.nih.gov/365706

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12 December 2020

Genetic and clinical study of a family of 7 children in which 3 persons have "crying cat syndrome"

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

DELETION OF SHORT ARM OF CHROMOSOME 5

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

"CRI DU CHAT" SYNDROME. A NEW CLINICAL AND CYTOGENETIC ENTITY

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

A partial trisomy 5p syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Cri-du-chat syndrome--an unhelpful designation

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Triosephosphate Isomerase Gene not Localized on the Short Arm of Chromosome 5 in Man

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Cri-du-chat syndrome in a 10 year old girl with deletion of the short arms of chromosome number 5. Observations on dermatoglyphics, maxillo-mandibular measurements and sound spectrograms

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Cri du chat syndrome [46, XY, 5p-] with balanced B/F translocation in father and grandfather: a case report.

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Reciprocal translocation t (5p--;19p+) in three generations (author's transl)

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Studies on human triosephosphate isomerase. 3. Characterization of the enzyme from patients with the cri du chat syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Crying cat syndrome in a 4-month-old infant

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Cri du chat: clinical and cytogenetic findings in two older patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Crying cat syndrome (partial deletion of the short arm of chromosome 5)

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Autosomal imbalance and its syndromes, excluding down's

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

A case of cri-du-chat associated with cataracts and transmitted from a mother with a 4-5 translocation

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

The cri-du-chat syndrome with an apparently normal karyotype

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

On the possible localization of a gene for triosephosphate isomerase on the short arm of human chromosome 5

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Defects in granulocyte function in various chromosome abnormalities (down's-, edwards'-, cri-du-chat syndrome)

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Spectrographic analysis of cries from children with maladie du cri du chat

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

[4 p- and 5 p- chromosome deletions]

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Cytologic observations in 35 individuals with a 5p- karyotype

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Cri-du-chat syndrome combined with partial C-group trisomy

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Cytogenetic study of a 5/14 translocation in man

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Reverse type of cri du chat disease: 5 p trisomy

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Partial deletion of short arm of a chromosome of the 4-5 group (Denver) in an adult male

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

5-21-22 translocation and the crying cat syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Cri-du-chat and trisomy 13 syndromes in an infant with an unbalanced chromosomal translocation

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Pseudohypoparathyroidism associated with cri du chat syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Familial segregation of a t(5p-;13q+). Complementary analysis from specimens preserved in liquid nitrogen

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

"Cri du chat" syndrome with maternal insertional translocation

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Hypertonia and the cat-cry syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Prenatal detection of crying cat syndrome due to balanced translocation in one parent

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

THE CRYING CAT SYNDROME

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

CHROMOSOMAL AUTORADIOGRAPHY IN THE CRI DU CHAT SYNDROME

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Observations on mosaicism in the crying cat syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Clustering in deleted short-arm length among 25 cases with a Bp– chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

[Crying cat disease associated with complex chromosome rearrangement in a dizygotic twin]

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Translocation heterozygosis: a cause of five cases of the cri du chat syndrome and two cases with a duplication of chromosome number five in three families

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

https://pubmed.ncbi.nlm.nih.gov/365706

1 reference

12 December 2020

Partial deletions and trisomies of chromosome 13; Mapping of bands associated with particular malformations

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

A new morbid state connected with a chromosome abnormality: Ehlers-Danlos syndrome associated with the "crying cat" disease in a newborn infant

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Cri-du-chat syndrome. Case report

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

FAMILIAL SEGREGATION OF A 5-13 TRANSLOCATION DETERMINING PARTIAL MONOSOMY AND A TRISOMY OF THE SHORT ARM OF THE 5 CHROMOSOME: "CAT CRY" DISEASE AND ITS "RECEPROCAL"

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Chromosome delection point in "cri du chat" syndrome (author's transl)

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

A comparison of the syneromes associated with a partial deletion of the short arms of chromosomes number 4 and number 5

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Crying cat syndrome. Case report

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Ocular Abnormalities in the Cri Du Chat Syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

On the localization of genes on certain autosomes of man through chromosome aberrations. 3. Exclusion of the possibility of gene assignment

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Cytogenetic survey of a hospital for the mentally retarded

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Mental retardation in the crying cat syndrome. Comparison of the intellectual level in the partial deletion of the short arm of chromosome 5 with trisomy 21 and deletions of chromosome 18. Apropos of 118 cases taken from the literature

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

LE CRI DU CHAT (CRYING CAT) SYNDROME.

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

[One-year psychological follow-up of 3 brothers with crying cat syndrome. Effect of the administration of neuroleptics on the course of the disease]

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Probable Localization of a Triosephosphate Isomerase Gene to the Short Arm of the Number 5 Human Chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

A comment to the paper: Localization exclusion of the HL-A genes from the short arm of human chromosome 5

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Possible localisation of the gene for cystic fibrosis of the pancreas to the short arm of chromosome 5.

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

The deletion of the short arms of a group 4-5 chromosome. Study of a case

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Partial monosomy 22 as the result of an unbalanced translocation 5:22 in a patient with cri-du-chat syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

[The crying cat syndrome. Description of a case]

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

[The crying cat syndrome]

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Hypertonia in older patients with the 5p-syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

A syndrome secondary to an aberration of chromosome 5, group B

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Chromosome aberrations in 2159 consecutive newborn babies

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Partial B trisomy in cat-cry-syndrome (author's transl)

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Mewing cry in a child with the partial deletion of the short arm of chromosome No. 4

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Trisomy 10p due to t(5;10)(p15;p11) segregating in a large sibship

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Localisation of the cystic-fibrosis gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

A family with balanced translocation, t(5p-;Gp+)

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Contribution to the clinical differential diagnosis of the crying cat syndrome. The results of an acoustic analysis of the "crying cat" and similar sounding infants' cries

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Neurological abnormalities in the `cri-du-chat' syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Identification of 2 familial translocations

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Chromosome mosaicism in a child with features characteristic of the 'Cat Cry' syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

A chromosome survey of a population of mentally retarded persons

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Skeletal Changes in the «Cri du Chat» Syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Distinction between chromosome 4 and chromosome 5 by replication pattern and length of long and short arms

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Inherited pericentric inversion of chromosome 5: a family with history of neonatal death and a case of the "cri du chat" syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

A pericentric inversion, 5p–q+, and additional complex rearrangements in a case of cri-du-chat syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

PARTIAL DELETION OF THE SHORT ARM OF CHROMOSOME 5. "LE CRI DU CHAT". ANOTHER EXAMPLE

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Deletion - translocation del (12) (p11) leads to (t10;12) (p13;pII)

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Cir-du-chat syndrome with an increased level of proline and threonine

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

[On a case of crying cat syndrome with apparently normal karyotype]

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

B group short-arm deletion syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

The Cri du Chat syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Translocation Y/5 resulting in Cri du Chat syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Transmission of the cri-du-chat syndrome from a maternal balanced translocation carrier, t(5p-;11q+)

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

PARTIAL DELETION OF SHORT ARMS OF CHROMOSOME NO. 5. REPORT OF A CASE IN A FRATERNAL TWIN.

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

The cri du chat syndrome in adolescents and adults: Clinical finding in 13 older patients with partial deletion of the short arm of chromosome No. 5(5p-)

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Structural aberrations of autosomes in a mentally retarded population.

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Facial appearance in cri du chat syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Screening for minute deletions in patients with suspected cri-du-chat syndrome and apparently normal karyotype

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

3 CASES OF PARTIAL DELETION OF THE SHORT ARM OF A 5 CHROMOSOME

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

PARTIAL DELETION OF THE SHORT ARM OF CHROMOSOME 5. INDIVIDUALIZATION OF A NEW MORBID STATE

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Cri-du-chat with chromosomal mosaicism

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Dermatoglyphics in Cri du Chat syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Alternative DNA replication patterns associated with long arm length of chromosomes 4 and 5 in the cri du chat syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Cytogenetic survey of 504 mentally retarded individuals

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

The cat cry syndrome (5p-) in adolescents and adults

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Analysis of the voice in a case of "crying cat disease"

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Crying cat syndrome with ring shaped chromosome 5

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Localization exclusion of the HL-A genes from the short arm of human chromosome 5

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

An autopsy case of cri du chat syndrome: The fifth case report of ring chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

PARTIAL DELETION OF THE SHORT ARM OF THE 5 CHROMOSOME: THE 5TH CASE OF CRYING CAT SYNDROME

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Cri-du-chat syndrome. A case report with spectral analysis of the "meowing"

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Comparative study of sole patterns in chromosomal abnormalities

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

A 45,XY,5-15-,t(5q15q) cri-du-chat child

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Cervical hernia of the lung associated with the cri du chat syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

AUTOSOMAL ABNORMALITIES

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Reciprocal translocations

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Chromosome survey of moderately to profoundly retarded patients.

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

"Cri du Chat" due to a ring-B chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

A case of crying cat syndrome. Partial deletion of the short arm of chromosome 5

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

The larynx in the cri du chat (cat cry) syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Psychopathological diagnostic error in a case of crying cat's syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Intrauterine growth in length and head circumference as estimated from live births at gestational ages from 26 to 42 weeks

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Study of the radiological signs of crying cat syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

A case of 'cri du chat' syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

A typical case of crying cat disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Combination of Goldenhar's syndrome with the Cri-Du-Chat syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Another "Cri-Du-Chat"

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Chromosome studies in full-term, low-birth-weight, mentally retarded patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Partial deletion of short arms in chromosomes from group B with translocation to group D in the father of children with multiple developmental anomalies

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

[Crying cat syndrome (5p-) with cleft palate]

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Chromosome survey of total population of mentally subnormal in North-East of Scotland

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

[Cri du chat syndrome]

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Karyotype with chromosomal abnormality with various inherited defects in the offspring (Recombination aneusomy)

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

"Cri du Chat" syndrome. Report of a case

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

INTRAUTERINE GROWTH AS ESTIMATED FROM LIVEBORN BIRTH-WEIGHT DATA AT 24 TO 42 WEEKS OF GESTATION

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Protein polymorphisms in a family with accumulated chromosome aberrations

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Case study: a premature baby with cri-du-chat syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Abnormalities in the field of otorhinolaryngology. Genetic report

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Prenatal diagnosis of 5p-

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

SOME NEW DATA ON AUTOSOMAL ABERRATIONS IN MAN

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Crying cat syndrome with chromosome mosaicism 46,XY-46,XY,5p-

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

The clinical and cytogenetic manifestations of four cases with partial deletion of the short arm of one of the chromosomes of group B

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Duplication deficiency syndrome in familial translocation (2q-; 5p+)

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Chromosome survey of a hospital for the mentally subnormal. 2. Autosome abnormalities.

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Identification of the abnormal B group chromosome in the "cri du chat" syndrome by QM-fluorescence

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

[Clinical and genetic studies of a patient with crying cat syndrome]

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

[Crying cat syndrome (apropos of a case)]

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

"Cri du chat" (cat cry) syndrome in Singapore

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Crying cat syndrome in a premature infant

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

[The clinical manifestations and cytogenetic observations of 7 cases affected by the cri-du-chat syndrome]

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Red-cell triosephosphate isomerase and chromosome 5

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

["Crying cat", a new malformation syndrome as a sequel to a chromosome abnormality (deficiency of the short arm of chromosome No. 5)]

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

De novo appearance of a translocation t(5p; 2Iq), and its transmission in both balanced and unbalanced forms to the next generation

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Localisation of the cystic-fibrosis gene.

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

5 cases of cri-du-chat syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Cri-Du-Chat syndrome in a child with a 46,XX,der(5),t(4;5)(q32;p14)pat Karyotype

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Deficiency in the short arms of Group B (4p--; 5p--) chromosomes. Studies on 6 patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

[Studies of the DNA replication pattern of the chromosome groups 4-5, 13-15 and 21-22 in invitro cultured human leukocytes]

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Partial deletion of the short branch of chromosome 5 (a new case: Pathological Anatomy Week, October 1965)

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

THE CRYING CAT SYNDROME: A FURTHER CASE

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Topological classification of palmar dermatoglyphics

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Partial trisomy 5 with a carrier parent t(5p‐;9p+)

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

'Cri-du-chat' syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

"Cri du chat" syndrome with additional physical findings of trisomy 17-18

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Apparent cri-du-chat and "antimongolism" in one patient

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

On the symptoms and cytogenetics of a further case of crying cat syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

A 45, XX,5–,13–, dic+ karyotype in a case of cri-du-chat syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

https://pubmed.ncbi.nlm.nih.gov/365706

1 reference

12 December 2020

Autosomal deletions 46,XY,del(12)(p11) and 46,XY-46,XY,del(5)(p13) with no effect on physical or mental development.

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

The cri du chat syndrome: neuropathologic observations

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

PARTIAL DELETION OF THE SHORT ARMS OF A CHROMOSOME OF THE 4-5 GROUP (DENVER).

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

3 children with crying cat syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

"Cri du chat" syndrome. Partial deletion of the short arm of a chromosome No. 5. Report of a case

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

The crying cat syndrome and its reciprocal

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Detection of minute deletions in human karyotypes

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Cri du chat syndrome and translocation t(5p--;18p+)

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Crying cat syndrome in 2 children

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

The chromosomal syndromes (author's transl)

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Clinical and genetic study of the "crying cat" syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/365706

12 December 2020

Identifiers

DOI

10.1007/BF00394291

1 reference

Dimensions Publication ID

4 August 2017

1030790210

0 references

1 reference