(Q35198592)

English

Analysis of DNA polymorphisms suggests that most de novo dup(21q) chromosomes in patients with Down syndrome are isochromosomes and not translocations

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scholarly article

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Europe PubMed Central

PubMed publication ID

7 August 2017

Analysis of DNA polymorphisms suggests that most de novo dup(21q) chromosomes in patients with Down syndrome are isochromosomes and not translocations (English)

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

1 reference

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author name string

Antonarakis SE

1

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

Adelsberger PA

2

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

Petersen MB

3

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

Binkert F

4

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Europe PubMed Central

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7 August 2017

Schinzel AA

5

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Europe PubMed Central

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7 August 2017

language of work or name

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publication date

1 December 1990

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Europe PubMed Central

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7 August 2017

American Journal of Human Genetics

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Europe PubMed Central

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7 August 2017

47

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Europe PubMed Central

PubMed publication ID

7 August 2017

6

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

968-972

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683910

13 July 2018

Evidence for reduced recombination on the nondisjoined chromosomes 21 in Down syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683910

13 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683910

13 July 2018

Hypervariabflity of simple sequences as a general source for polymorphic DNA markers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683910

13 July 2018

A hypervariable microsatellite revealed by in vitro amplification of a dinucleotide repeat within the cardiac muscle actin gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683910

13 July 2018

Isochromosome not translocation in trisomy 21q21q

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683910

13 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683910

13 July 2018

The polydeoxyadenylate tract of Alu repetitive elements is polymorphic in the human genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683910

13 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683910

13 July 2018

Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683910

13 July 2018

Epidemiological aspects of trisomy 21

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683910

13 July 2018

Molecular evidence for true isochromosome 21q

1 reference

https://pubmed.ncbi.nlm.nih.gov/1978562

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage analysis of the human HMG14 gene on chromosome 21 using a GT dinucleotide repeat as polymorphic marker

1 reference

https://pubmed.ncbi.nlm.nih.gov/1978562

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A genetic linkage map of 17 markers on human chromosome 21

1 reference

https://pubmed.ncbi.nlm.nih.gov/1978562

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

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