(Q35195088)

7 August 2017

title

Down syndrome: molecular mapping of the congenital heart disease and duodenal stenosis (English)

1 reference

7 August 2017

0 references

1 reference

congenital heart disease

1 reference

1 reference

Korenberg JR

1

1 reference

7 August 2017

Bradley C

series ordinal

2

1 reference

7 August 2017

Disteche CM

series ordinal

3

1 reference

7 August 2017

language of work or name

English

0 references

publication date

1 February 1992

1 reference

American Journal of Human Genetics

7 August 2017

published in

1 reference

7 August 2017

volume

50

1 reference

7 August 2017

issue

2

1 reference

7 August 2017

page(s)

294-302

1 reference

Nucleotide sequence and expression of human chromosome 21-encoded superoxide dismutase mRNA.

7 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=1682442

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

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682442

Isolation of polymorphic DNA segments from human chromosome 21.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682442

Cloned DNA probes regionally mapped to human chromosome 21 and their use in determining the origin of nondisjunction

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682442

Variable number of tandem repeat (VNTR) markers for human gene mapping

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682442

RFLPS at the D21S19 locus of human chromosome 21.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682442

Amyloid beta protein gene: cDNA, mRNA distribution, and genetic linkage near the Alzheimer locus

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682442

Comparative mapping of DNA markers from the familial Alzheimer disease and Down syndrome regions of human chromosome 21 to mouse chromosomes 16 and 17

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682442

Isolation and regional mapping of DNA sequences unique to human chromosome 21.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682442

Molecular genetic approach to the characterization of the "Down syndrome region" of chromosome 21.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682442

The Alzheimer amyloid precursor protein maps to human chromosome 21 bands q21.105-q21.05.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682442

Critical role of the D21S55 region on chromosome 21 in the pathogenesis of Down 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=1682442

Free proximal trisomy 21 without the Down 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=1682442

Physical mapping around the Alzheimer disease locus on the proximal long arm of chromosome 21

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682442

Analysis of human chromosome 21: correlation of physical and cytogenetic maps; gene and CpG island distributions

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682442

Molecular definition of a region of chromosome 21 that causes features of the Down syndrome phenotype

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682442

High Resolution of 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=1682442

Partial trisomy 21 (21q21 - 21q22.2)

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682442

Trisomy 16 in the mouse fetus associated with generalized edema and cardiovascular and urinary tract anomalies.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682442

The mouse neurological mutant weaver maps within the region of chromosome 16 that is homologous to human chromosome 21

27 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/1531166

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

A boy with Down's syndrome having recombinant chromosome 21 but no SOD-1 excess

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/1531166

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

PMC publication ID

1682442

1 reference

7 August 2017

1 reference