(Q35889069)

10 August 2017

Understanding the mechanism(s) of mosaic trisomy 21 by using DNA polymorphism analysis (English)

1 reference

10 August 2017

C Pangalos

1

1 reference

10 August 2017

D Avramopoulos

2

1 reference

10 August 2017

J L Blouin

3

1 reference

10 August 2017

O Raoul

4

1 reference

10 August 2017

M C deBlois

5

1 reference

10 August 2017

M Prieur

6

1 reference

10 August 2017

A A Schinzel

7

1 reference

10 August 2017

M Gika

8

1 reference

10 August 2017

D Abazis

9

1 reference

10 August 2017

S E Antonarakis

10

1 reference

10 August 2017

language of work or name

English

0 references

publication date

1 March 1994

1 reference

American Journal of Human Genetics

10 August 2017

1 reference

10 August 2017

54

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10 August 2017

3

1 reference

10 August 2017

473-481

1 reference

Study of somatic chromosomes from 9 mongoloid children

10 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918141

Human chromosome 21: genome mapping and exploration, circa 1993.

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918141

Maternal uniparental disomy for human chromosome 14, due to loss of a chromosome 14 from somatic cells with t(13;14) trisomy 14.

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918141

Normal phenotype with paternal uniparental isodisomy for chromosome 21.

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918141

The origin of mosaic Down syndrome: four cases with chromosome markers

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918141

Enzymatic amplification of beta-globin genomic sequences and restriction site analysis for diagnosis of sickle cell anemia

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918141

Abundant class of human DNA polymorphisms which can be typed using the polymerase chain reaction

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918141

Maternal origin of a de novo balanced t(21q21q) identified by ets-2 polymorphism

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918141

Familial sex chromosomal mosaicism

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918141

Origin of extra chromosome 21 in 343 families: cytogenetic and molecular approaches

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918141

Trisomy 21: association between reduced recombination and nondisjunction

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918141

Use of short sequence repeat DNA polymorphisms after PCR amplification to detect the parental origin of the additional chromosome 21 in Down syndrome

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918141

DNA polymorphism analysis in families with recurrence of free trisomy 21

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918141

Comparative study of microsatellite and cytogenetic markers for detecting the origin of the nondisjoined chromosome 21 in Down syndrome

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918141

The meiotic stage of nondisjunction in trisomy 21: determination by using DNA polymorphisms

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918141

Down syndrome: Cytogenetical epidemiology

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918141

Mitotic errors in somatic cells cause trisomy 21 in about 4.5% of cases and are not associated with advanced maternal age

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918141

Parental origin of the extra chromosome in trisomy 21 as indicated by analysis of DNA polymorphisms. Down Syndrome Collaborative Group

14 November 2018

1 reference

PubMed

12 December 2020

A Linkage Map of Human Chromosome 21: 43 PCR Markers at Average Intervals of 2.5 cM

1 reference

PubMed

12 December 2020

Cell Selection in vivo in Normal/G Trisomic Mosaics

1 reference

PubMed

12 December 2020

1 reference

12 December 2020

Identifiers

1 reference

10 August 2017

PubMed publication ID

8116616

1 reference