(Q34529606)

2 August 2017

title

Nonrandom distribution of exchange points in patients with structural rearrangements (English)

1 reference

2 August 2017

main subject

chromosome abnormality

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1247018

8 November 2023

crossing over

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1247018

8 November 2023

author name string

Y. Nakagome

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1247018

8 November 2023

H. Chiyo

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1247018

8 November 2023

language of work or name

English

0 references

publication date

1 January 1976

1 reference

full work available at URL

2 August 2017

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/1247018/?tool=EBI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1247018

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/1247018/pdf/?tool=EBI

8 November 2023

file format

Portable Document Format

online access status

open access

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1247018

https://europepmc.org/articles/PMC1684910

8 November 2023

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1247018

https://europepmc.org/articles/PMC1684910?pdf=render

8 November 2023

file format

Portable Document Format

online access status

open access

content deliverer

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1247018

American Journal of Human Genetics

8 November 2023

published in

1 reference

2 August 2017

volume

28

1 reference

2 August 2017

issue

1

1 reference

2 August 2017

page(s)

31-41

1 reference

Preferential location of x-ray induced chromosome breakage in the R-bands of human chromosomes

2 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684910

Three translocations involving C- or G-group chromosomes

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684910

High resolution studies on the pattern of induced exchanges in the human karyotype

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684910

Radiation-induced non-random chromosome breakage

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684910

Heterozygosity and homozygosity for a pericentric inversion of human chromosone 3

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684910

Familial translocation t(4;22) (p11;p12) and trisomy 4p in 2 sisters

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684910

Trisomy 4p due to recombination aneusomy of an inversion 4 (p 14, q 35)

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684910

[Partial trisomy 10q dueto familial translocation t(10q-; 22p-plus)]

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684910

T (14q-; 21q + ) translocation in the father. Partial trisomy 14 and monosomy 21 in the daughter

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684910

Partial trisomy 4p with translocation 4p-, 22p+ in the father.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684910

Assignment by Deletion of Human Red Cell Acid Phosphatase Gene Locus to the Short Arm of Chromosome 2

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684910

Partial trisomy 8 (8q24) and the trisomy-8 syndrome.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684910

Precise identification of various chromosomal abnormalities.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684910

Position of the Duffy locus on chromosome 1 in relation to breakpoints for structural rearrangements

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684910

Distribution of mitomycin C-induced damage in human chromosomes with special reference to regions of repetitive DNA.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684910

Tentative localization of a Hageman (Factor XII) locus on 7q, probably the 7q35 band

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684910

Pericentric inversions of human chromosomes 9 and 10.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684910

Partial trisomy 12 in a mentally retarded boy and translocation (12;21) in his mother

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684910

Inherited partial duplication of chromosome No. 15.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684910

Different forms of incomplete trisomy 13. Mosaicism and partial trisomy for the proxim

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684910

Translocation, t(4qminus;13qplus), in three generations resulting in partial trisomy of the long arm of chromosome 4 in the fourth generation

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684910

Autosomal reciprocal translocations in newborn children and their relatives

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684910

[Inherited translocation t(4q minus;18q plus) with unbalanced progeny of different types (author's transl)].

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684910

Localization of sister chromatid exchanges in human chromosomes

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684910

An analysis of the break points of structural rearrangements in man

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684910

An (11;21) translocation in four generations with chromosome 11 abnormalities in the offspring. A clinical, cytogenetical, and gene marker study

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684910

Trisomy 13 with a 13-X translocation

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684910

Chromosome abnormality and perinatal death

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684910

Segregating reciprocal (4;21) (q21;q21) translocation with proposita trisomic for parts of 4q and 21.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684910

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684910

Partial trisomy 8: trisomy of the distal part of the long arm of chromosome number 8 plus (8q2) in a severely retarded and malformed girl.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684910

Identification of a large submetacentric X chromosome as pericentric inversion of an isochromosome of the long arm

27 October 2018

1 reference

https://pubmed.ncbi.nlm.nih.gov/1247018

12 December 2020

Familial balanced translocation t(2; 13) (q32; q33) and partial trisomy 2q

1 reference

https://pubmed.ncbi.nlm.nih.gov/1247018

12 December 2020

[Translocation 46,XX, t(15; 21) (q13; q22,1) in the mother of 2 children with partial trisomy 15 and monosomy 21]

1 reference

https://pubmed.ncbi.nlm.nih.gov/1247018

12 December 2020

Pericentric inversion of chromosome 4 : inv (4) (p13, q35) and trisomy of the short branch of chromosome 4 due to recombination aneusomy

1 reference

https://pubmed.ncbi.nlm.nih.gov/1247018

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/1247018

12 December 2020

Evidence for an inverse relationship between X-ray induced chromatid and chromosome breakage in human chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/1247018

12 December 2020

Segregation of genetic markers in families with chromosome polymorphisms and structural rearrangements involving chromosome 1

1 reference

https://pubmed.ncbi.nlm.nih.gov/1247018

12 December 2020

Translocation 8-22 with no length change and partial trisomy for 8q. Detection by heat denaturation

1 reference

https://pubmed.ncbi.nlm.nih.gov/1247018

12 December 2020

Points of exchange in a human no. 5 ring chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/1247018

12 December 2020

Microdensitometric identification of the pericentric inversion of chromosome No.2 and of duplication of the short arm of chromosome No.7 in a reexamined case

1 reference

https://pubmed.ncbi.nlm.nih.gov/1247018

12 December 2020

Trisomy for short arm of chromosome 20

1 reference

https://pubmed.ncbi.nlm.nih.gov/1247018

12 December 2020

Rare translocation 47,XY,t(12;21) in Down's syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/1247018

12 December 2020

Partial 7q trisomy due to t(7;12) (q22;q24) familial translocation

1 reference

https://pubmed.ncbi.nlm.nih.gov/1247018

12 December 2020

https://pubmed.ncbi.nlm.nih.gov/1247018

1 reference

12 December 2020

Translocation heterozygosity and associated subfertility in man

1 reference

https://pubmed.ncbi.nlm.nih.gov/1247018

12 December 2020

Autoradiographically identified karyotype 49,XXXXY, t(4; 11) (q35; q23) confirmed by banding

1 reference

https://pubmed.ncbi.nlm.nih.gov/1247018

12 December 2020

Partial trisomy 14 following a balanced reciprocal translocation t(14q-;21q+)

1 reference

https://pubmed.ncbi.nlm.nih.gov/1247018

12 December 2020

Brother and sister with trisomy 10p: a new syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/1247018

12 December 2020

Banding patterns and autoradiographic studies of cells with an X-autosome translocation

1 reference

https://pubmed.ncbi.nlm.nih.gov/1247018

12 December 2020

Unbalanced X-autosomal translocation with inactivation of the normal X chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/1247018

12 December 2020

Identifiers

PMC publication ID

1684910

1 reference

2 August 2017

1 reference