(Q33669486)

28 July 2017

Down's syndrome phenotype and autosomal gene inactivation in a child with presumed (X;21) de novo translocation (English)

1 reference

28 July 2017

Taysi K

1

1 reference

28 July 2017

Sparkes RS

series ordinal

2

1 reference

28 July 2017

O'Brien TJ

series ordinal

3

1 reference

28 July 2017

Dengler DR

series ordinal

4

1 reference

28 July 2017

language of work or name

English

0 references

publication date

1 April 1982

1 reference

Journal of Medical Genetics

28 July 2017

1 reference

28 July 2017

19

1 reference

28 July 2017

144-148

1 reference

28 July 2017

2

1 reference

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

28 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048847

Trisomy 13 with a 13-X translocation

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048847

Human X-autosome translocations: differential inactivation of the X chromosome in a kindred with an X-9 translocation

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048847

A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048847

Replication pattern of the X chromosomes in three X/autosomal translocations.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048847

X-autosome translocations: a review

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048847

Spreading of inactivation in an (X;14) translocation

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048847

Evidence for a correlation between late replication and autosomal gene inactivation in a familial translocation t(X;21)

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048847

A diagnostic index for Down syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048847

Down syndrome due to partial trisomy 21q

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048847

Clinical diagnosis of Down's syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048847

Dermatoglyphic nomogram for the diagnosis of Down's syndrome

21 June 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/6210775

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Trisomy 21 and superoxide dismutase-1 (IPO-A). Tentative localization of sub-band 21Q22.1

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/6210775

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

PMCID

1048847

1 reference

28 July 2017

1 reference