(Q35201743)

7 August 2017

Unstable familial translocations: A t(11;22)mat inherited as a t(11;15) (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7294023

human chromosomes 6-12 and X

19 April 2024

main subject

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7294023

19 April 2024

human chromosomes 13-15

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7294023

chromosomal translocation

19 April 2024

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7294023

19 April 2024

author name string

D. J. Tomkins

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7294023

19 April 2024

language of work or name

English

0 references

publication date

1 September 1981

1 reference

full work available at URL

7 August 2017

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/7294023/?tool=EBI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7294023

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/7294023/pdf/?tool=EBI

19 April 2024

file format

Portable Document Format

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7294023

https://europepmc.org/articles/PMC1685141

19 April 2024

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7294023

https://europepmc.org/articles/PMC1685141?pdf=render

19 April 2024

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%3A7294023

American Journal of Human Genetics

19 April 2024

published in

1 reference

7 August 2017

33

1 reference

7 August 2017

745-751

1 reference

7 August 2017

5

1 reference

Partial 3p trisomy and different rearrangements involving chromosome 3 in the proposita's family

7 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685141

A family with two translocations and a polymorphism involving chromosome 14.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685141

A human family suggesting evidence for centric fission and stability of a telocentric chromosome.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685141

Down's syndrome associated with two Robertsonian translocations, 45,XX,-15,-21, + t(15q21q) and 46,XX,-21, + t(21q21q).

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685141

46,XY,21qi-46,XY,21p- mosaicism in a child with Down's syndrome.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685141

Distribution of spontaneous chromosome breaks in human chromosomes

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685141

The possibility of latent centromeres and a proposed nomenclature system for total chromosome and whole arm translocations

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685141

Mosaic 13 trisomy due to de novo 13/13 translocation with subsequent fission karyotype: 46,XX,-13,+t(13;13)(p11;q11)/46,XX,del(13)(p11)

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685141

A jumping translocation (5p;15q), (8q;15q), and (12q;15q) (author's transl)

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685141

Telomere replication, kinetochore organizers, and satellite DNA evolution

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685141

Unstable telocentric chromosome produced after centric misdivision of a 21q/21q translocated element

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685141

Dissociation as probable origin of mosaic 45,XY,t(15;21)/46,XY,i(21q)

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685141

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

13 July 2018

1 reference

12 December 2020

A case of centric fission in man

1 reference

12 December 2020

Centric fission of chromosome No. 4 in the mother of two patients with trisomy 4p

1 reference

12 December 2020

Nonrandom distribution of chromosome breaks in cultured lymphocytes of normal subjects

1 reference

12 December 2020

"Jumping" satellites in three generations: a warning for paternity tests and prenatal diagnosis

1 reference

12 December 2020

A cytogenetic survey of 14,069 newborn infants. III. an analysis of the significance and cytologic behavior of the Robertsonian and reciprocal translocations

1 reference

12 December 2020

Balanced transmission of centromeric fission products in man

1 reference

12 December 2020

Prader-Willi syndrome and a bisatellited derivative of chromosome 15

1 reference

12 December 2020

An extra idic(15p)(q11) chromosome in Prader-Willi syndrome

1 reference

12 December 2020

Identifiers

PMCID

1685141

1 reference

7 August 2017

1 reference