The meiotic stage of nondisjunction in trisomy 21: determination by using DNA polymorphisms (Q35199335)

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18 September 2019

title

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

1 reference

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18 September 2019

author name string

S. E. Antonarakis

1

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16 September 2022

M. B. Petersen

2

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16 September 2022

M. G. McInnis

3

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16 September 2022

P. A. Adelsberger

4

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16 September 2022

A. A. Schinzel

5

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16 September 2022

F. Binkert

6

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16 September 2022

C. Pangalos

7

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16 September 2022

O. Raoul

8

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16 September 2022

S. A. Slaugenhaupt

9

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16 September 2022

M. Hafez

10

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16 September 2022

publication date

1 March 1992

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https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/1347192/?tool=EBI

18 September 2019

language of work or name

English

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work available at URL

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https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/1347192/pdf/?tool=EBI

16 September 2022

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https://europepmc.org/articles/PMC1684265

16 September 2022

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https://europepmc.org/articles/PMC1684265?pdf=render

16 September 2022

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American Journal of Human Genetics

16 September 2022

published in

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18 September 2019

volume

50

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18 September 2019

issue

3

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18 September 2019

page(s)

544-550

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18 September 2019

1 reference

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13 July 2018

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

13 July 2018

1 reference

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Homologous subfamilies of human alphoid repetitive DNA on different nucleolus organizing chromosomes

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Efficient computations in multilocus linkage analysis

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Mitotic recombination in yeast

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

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Analysis of DNA haplotypes suggests a genetic predisposition to trisomy 21 associated with DNA sequences on chromosome 21

13 July 2018

1 reference

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

13 July 2018

1 reference

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Trisomy 21 (Down syndrome): studying nondisjunction and meiotic recombination by using cytogenetic and molecular polymorphisms that span chromosome 21.

13 July 2018

1 reference

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Dinucleotide repeat polymorphism located at D21S120.

13 July 2018

1 reference

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

13 July 2018

1 reference

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

13 July 2018

1 reference

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Dinucleotide repeat polymorphism at the D21S13E locus

13 July 2018

1 reference

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Centre d'etude du polymorphisme humain (CEPH): collaborative genetic mapping of the human genome

13 July 2018

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Dinucleotide repeat polymorphism at the D21S172 locus

13 July 2018

1 reference

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Genetics and biology of human ovarian teratomas. II. Molecular analysis of origin of nondisjunction and gene-centromere mapping of chromosome I markers

13 July 2018

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PCR detection of two RFLP's at the D21S13 locus

13 July 2018

1 reference

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Trisomy 21: association between reduced recombination and nondisjunction

13 July 2018

1 reference

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

13 July 2018

1 reference

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A genetic linkage map of 27 markers on human chromosome 21

13 July 2018

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1 reference

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1 reference

12 December 2020

Alphoid DNA polymorphisms for chromosome 21 can be distinguished from those of chromosome 13 using probes homologous to both

1 reference

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

1 reference

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Non-disjunction in trisomy 21: study of chromosomal heteromorphisms in 110 families

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Identifiers

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18 September 2019

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