(Q35570666)

English

Familial Down syndrome due to t(10;21) translocation: evidence that the Down phenotype is related to trisomy of a specific segment of chromosome 21

scientific article published on July 1, 1975

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scholarly article

1 reference

Europe PubMed Central

8 August 2017

Familial Down syndrome due to t(10;21) translocation: evidence that the Down phenotype is related to trisomy of a specific segment of chromosome 21 (English)

1 reference

Europe PubMed Central

8 August 2017

1 reference

based on heuristic

inferred from title

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based on heuristic

inferred from title

human chromosomes 6-12 and X

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A125542

6 December 2022

chromosome abnormality

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A125542

6 December 2022

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A125542

6 December 2022

chromosomal translocation

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A125542

6 December 2022

author name string

J. D. Williams

1

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A125542

6 December 2022

R. L. Summitt

2

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A125542

6 December 2022

P. R. Martens

3

1 reference

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A125542

6 December 2022

R. A. Kimbrell

4

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A125542

6 December 2022

language of work or name

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publication date

1 July 1975

1 reference

Europe PubMed Central

8 August 2017

number of pages

8

1 reference

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inferred from page(s)

full work available at URL

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/125542/?tool=EBI

online access status

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A125542

6 December 2022

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/125542/pdf/?tool=EBI

Portable Document Format

online access status

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A125542

6 December 2022

https://europepmc.org/articles/PMC1762808

online access status

content deliverer

Europe PubMed Central

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A125542

6 December 2022

https://europepmc.org/articles/PMC1762808?pdf=render

Portable Document Format

online access status

content deliverer

Europe PubMed Central

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A125542

6 December 2022

American Journal of Human Genetics

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Europe PubMed Central

8 August 2017

27

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Europe PubMed Central

8 August 2017

478-485

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Europe PubMed Central

8 August 2017

4

1 reference

Europe PubMed Central

8 August 2017

Down's syndrome. The possibility of a pathogenetic segment on chromosome no. 21.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762808

27 July 2018

A case of 47,XX,(21q-)+ with some stigmata of Down's syndrome and an IQ of 77.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762808

27 July 2018

An extra chromosomal centric fragment in an infant with stigmata of Down's syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762808

27 July 2018

Retardation in a child with an extra submetacentric chromosome fragment and partial mongolism.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762808

27 July 2018

A chromosomal abnormality in a girl with some features of Down's syndrome (mongolism)

1 reference

https://pubmed.ncbi.nlm.nih.gov/125542

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An unusual translocation in a case of Mongolism

1 reference

https://pubmed.ncbi.nlm.nih.gov/125542

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A PARTIAL MONGOL

1 reference

https://pubmed.ncbi.nlm.nih.gov/125542

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of G-group chromosomes involved in a G-G tandem-translocation by the giemsa-band technique

1 reference

https://pubmed.ncbi.nlm.nih.gov/125542

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Two subterminal heterochromatin regions in a rare form of 21-21 translocation]

1 reference

https://pubmed.ncbi.nlm.nih.gov/125542

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Partial trisomy 21

1 reference

https://pubmed.ncbi.nlm.nih.gov/125542

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Down's syndrome associated with a familial (21q-; 22q+) translocation

1 reference

https://pubmed.ncbi.nlm.nih.gov/125542

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A new case of incomplete Down syndrome with partial trisomy 21

1 reference

https://pubmed.ncbi.nlm.nih.gov/125542

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dermatoglyphic nomogram for the diagnosis of Down's syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/125542

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fluorescent chromosomes of a tandem translocation in a mongol patient

1 reference

https://pubmed.ncbi.nlm.nih.gov/125542

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A Gq deletion in a girl with Down's syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/125542

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A case of G-G translocation in tandem

1 reference

https://pubmed.ncbi.nlm.nih.gov/125542

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Incomplete trisomy in a mongoloid child exhibiting minimal stigmata

1 reference

https://pubmed.ncbi.nlm.nih.gov/125542

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A chromosome abnormality with fragment in a paramongol child

1 reference

https://pubmed.ncbi.nlm.nih.gov/125542

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

1 reference

Europe PubMed Central

8 August 2017

1 reference

Europe PubMed Central

8 August 2017

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