Susceptible chiasmate configurations of chromosome 21 predispose to non-disjunction in both maternal meiosis I and meiosis II (Q71835124)

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21 October 2019

title

Susceptible chiasmate configurations of chromosome 21 predispose to non-disjunction in both maternal meiosis I and meiosis II (English)

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21 October 2019

8

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21 October 2019

author name string

Lamb NE

1

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21 October 2019

Freeman SB

2

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21 October 2019

Savage-Austin A

3

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21 October 2019

Pettay D

4

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21 October 2019

Taft L

5

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21 October 2019

Hersey J

6

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21 October 2019

Gu Y

7

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21 October 2019

Saker D

9

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21 October 2019

May KM

10

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21 October 2019

Avramopoulos D

11

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21 October 2019

Petersen MB

12

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21 October 2019

Hallberg A

13

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21 October 2019

Mikkelsen M

14

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Hassold TJ

15

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Sherman SL

16

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21 October 2019

publication date

1 December 1996

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21 October 2019

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21 October 2019

volume

14

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21 October 2019

page(s)

400-405

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21 October 2019

issue

4

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https://scigraph.springernature.com/pub.10.1038/ng1296-400

21 October 2019

exact match

0 references

cites work

Non-disjunction of chromosome 21 in maternal meiosis I: evidence for a maternal age-dependent mechanism involving reduced recombination

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

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

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

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Recombinationless meiosis in Saccharomyces cerevisiae

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ZIP1 is a synaptonemal complex protein required for meiotic chromosome synapsis

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Meiotic segregation in Drosophila melanogaster females: molecules, mechanisms, and myths

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Separation anxiety: the etiology of nondisjunction in flies and people.

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The origin of 47,XXY and 47,XXX aneuploidy: heterogeneous mechanisms and role of aberrant recombination

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7 January 2021

Analysis of non-disjunction in sex chromosome tetrasomy and pentasomy

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Sister-chromatid cohesion in mitosis and meiosis

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Etiology of nondisjunction in humans

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Chiasma frequency and maternal age in mammals.

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A Contiguous Physical Map of the Pericentromeric Region of Chromosome 21q between D21Z1 and D21S13E

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7 January 2021

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

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7 January 2021

Methods for studying recombination on chromosomes that undergo nondisjunction

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7 January 2021

A centromere map of the X chromosome from trisomies of maternal origin

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Multilocus recombination frequencies

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7 January 2021

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

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Construction of multilocus genetic linkage maps in humans

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MAP, an expert system for multiple pairwise linkage analysis.

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7 January 2021

Identifiers

DOI

10.1038/NG1296-400

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8944019%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

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