(Q68858398)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4442881%20AND%20SRC:MED&resulttype=core&format=json

28 September 2019

title

A pericentric inversion of a chromosome 4 with a t(4q+10p-) and a familial t(DqDq) in a mentally retarded girl (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4442881%20AND%20SRC:MED&resulttype=core&format=json

28 September 2019

author name string

S W Soukup

series ordinal

1

1 reference

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28 September 2019

W Yarema

series ordinal

2

1 reference

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28 September 2019

M Robinow

series ordinal

3

1 reference

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28 September 2019

publication date

1 January 1974

1 reference

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28 September 2019

1 reference

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28 September 2019

volume

25

1 reference

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28 September 2019

issue

1

1 reference

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28 September 2019

page(s)

69-78

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4442881%20AND%20SRC:MED&resulttype=core&format=json

Fertility in balanced heterozygotes for a familial centric fusion translocation, t(DgDg)

28 September 2019

cites work

1 reference

https://pubmed.ncbi.nlm.nih.gov/4442881

12 December 2020

A new syndrome resulting from partial trisomy for the distal third of the long arm of chromosome 10

1 reference

https://pubmed.ncbi.nlm.nih.gov/4442881

12 December 2020

Pericentric inversion of chromosome 9.

1 reference

https://pubmed.ncbi.nlm.nih.gov/4442881

12 December 2020

Double heteroploidy, 46, XY, t(13q14q), +18, in a spontaneous abortus

1 reference

https://pubmed.ncbi.nlm.nih.gov/4442881

12 December 2020

Chromosome aberrations and human diseases. XXY Klinefelter's syndrome from 46 chromosomes caused by T-T centromeric fusion

1 reference

https://pubmed.ncbi.nlm.nih.gov/4442881

12 December 2020

Reexamination of a family with a t(13q14q) and a ring D(13) child.

1 reference

https://pubmed.ncbi.nlm.nih.gov/4442881

12 December 2020

Identification of D-D translocations in mentally retarded patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/4442881

12 December 2020

Down's syndrome with a familial D/D reciprocal translocation and a G/G chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/4442881

12 December 2020

A t(13q14q) family with the translocation and a Philadelphia chromosome in one member.

1 reference

https://pubmed.ncbi.nlm.nih.gov/4442881

12 December 2020

Male infertility and 13-14 translocation

1 reference

https://pubmed.ncbi.nlm.nih.gov/4442881

12 December 2020

TWO LEUKEMIC PERIPHERAL BLOOD STEMLINES DURING ACUTE TRANSFORMATION OF CHRONIC MYELOGENOUS LEUKEMIA IN A D/D TRANSLOCATION CARRIER

1 reference

https://pubmed.ncbi.nlm.nih.gov/4442881

12 December 2020

Pericentric inversion of a group C autosome: a study of three families

1 reference

https://pubmed.ncbi.nlm.nih.gov/4442881

12 December 2020

Pericentric inversion, inv(10), in a mother and aneusomy by recombination, inv(10),rec(10), in her son

1 reference

https://pubmed.ncbi.nlm.nih.gov/4442881

12 December 2020

Chromosome preparations of leukocytes cultured from human peripheral blood

1 reference

https://pubmed.ncbi.nlm.nih.gov/4442881

12 December 2020

Quinacrine mustard fluorescence of human chromosomes: characterization of unusual translocations

1 reference

https://pubmed.ncbi.nlm.nih.gov/4442881

12 December 2020

Study of progeny of individuals bearing a t(DqDq) translocation

1 reference

https://pubmed.ncbi.nlm.nih.gov/4442881

12 December 2020

A suggestion for the nomenclature of the fluorescent banding patterns in human metaphase chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/4442881

12 December 2020

FAMILIAL MOSAICISM ATTRIBUTABLE TO A NEW GENE

1 reference

https://pubmed.ncbi.nlm.nih.gov/4442881

12 December 2020

Chromosomal Translocation in a Mentally Deficient Child with Cryptorchidism

1 reference

https://pubmed.ncbi.nlm.nih.gov/4442881

12 December 2020

2 familial translocations occurring together in each of 2 sisters, one balanced, the other partial trisomic 10q

1 reference

https://pubmed.ncbi.nlm.nih.gov/4442881

12 December 2020

Fertility and 13-14 translocation

1 reference

https://pubmed.ncbi.nlm.nih.gov/4442881

12 December 2020

Inherited translocations in two families (t(14q+;10q-) and t(13q-;21q+)).

1 reference

https://pubmed.ncbi.nlm.nih.gov/4442881

12 December 2020

Diverse chromosomal anomalies in a family

1 reference

https://pubmed.ncbi.nlm.nih.gov/4442881

12 December 2020

The use of proteolytic enzymes for the mapping of structural rearrangements in the chromosomes of man

1 reference

https://pubmed.ncbi.nlm.nih.gov/4442881

12 December 2020

Familial 13-15 translocation abnormality (Denver classification) associated with one case of cerebral palsy. Preliminary report

1 reference

https://pubmed.ncbi.nlm.nih.gov/4442881

12 December 2020

[Partial trisomy 10 due to hereditary translocation t(1;10)(q44;q22)]

1 reference

https://pubmed.ncbi.nlm.nih.gov/4442881

12 December 2020

NORMAL AND ABNORMAL INTERORBITAL DISTANCES, WITH SPECIAL REFERENCE TO MONGOLISM

1 reference

https://pubmed.ncbi.nlm.nih.gov/4442881

12 December 2020

Inherited pericentric inversion of chromosome no. 4.

1 reference

https://pubmed.ncbi.nlm.nih.gov/4442881

12 December 2020

Trisomy D1 with two D-D translocation chromosomes. Report of a case

1 reference

https://pubmed.ncbi.nlm.nih.gov/4442881

12 December 2020

A case of double aneuploidy, 47,XXY,14-,t(13q14q)+, also probably homozygous for the cystic fibrosis gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/4442881

12 December 2020

Chromosome studies in a neonatal population.

1 reference

https://pubmed.ncbi.nlm.nih.gov/4442881

12 December 2020

Transmission of a D/D reciprocal translocation in a family with high incidence of mental retardation

1 reference

https://pubmed.ncbi.nlm.nih.gov/4442881

12 December 2020

Chromosome studies in repeated spontaneous abortions and stillbirths.

1 reference

https://pubmed.ncbi.nlm.nih.gov/4442881

12 December 2020

The effects of various banding procedures on human chromosomes, studied with acridine orange

1 reference

https://pubmed.ncbi.nlm.nih.gov/4442881

12 December 2020

Partial deletion of the short arm of chromosome no. 4(4p-): clinical studies in five unrelated patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/4442881

12 December 2020

The chromosomal constitution of 165 human translocations involving D group chromosomes identified by autoradiography

1 reference

https://pubmed.ncbi.nlm.nih.gov/4442881

12 December 2020

Identifiers

1 reference