(Q35195059)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8352279%20AND%20SRC:MED&resulttype=core&format=json

30 October 2019

title

Nondisjunction of chromosome 15: origin and recombination (English)

1 reference

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30 October 2019

author name string

W P Robinson

1

1 reference

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30 October 2019

F Bernasconi

2

1 reference

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30 October 2019

A Mutirangura

3

1 reference

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30 October 2019

D H Ledbetter

4

1 reference

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30 October 2019

S Langlois

5

1 reference

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30 October 2019

S Malcolm

6

1 reference

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30 October 2019

M A Morris

7

1 reference

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30 October 2019

A A Schinzel

8

1 reference

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30 October 2019

language of work or name

English

0 references

publication date

1 September 1993

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8352279%20AND%20SRC:MED&resulttype=core&format=json

American Journal of Human Genetics

30 October 2019

published in

1 reference

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30 October 2019

volume

53

1 reference

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30 October 2019

issue

3

1 reference

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30 October 2019

page(s)

740-751

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8352279%20AND%20SRC:MED&resulttype=core&format=json

Non-Disjunction as Proof of the Chromosome Theory of Heredity (Concluded).

30 October 2019

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682425

EXCHANGE AND NONDISJUNCTION OF THE X CHROMOSOMES IN FEMALE DROSOPHILA MELANOGASTER

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682425

Multiplex PCR of three dinucleotide repeats in the Prader-Willi/Angelman critical region (15q11-q13): molecular diagnosis and mechanism of uniparental disomy.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682425

Methods for studying recombination on chromosomes that undergo 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=1682425

Origin of sex chromosome aneuploidy.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682425

Evidence for reduced recombination on the nondisjoined chromosomes 21 in 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=1682425

Genetic imprinting suggested by maternal heterodisomy in nondeletion Prader-Willi 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=1682425

The origin of aneuploidy: bivalent instability and the maternal age effect in trisomy 21 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=1682425

Chromosome synapsis and genetic recombination: their roles in meiotic chromosome segregation

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682425

Molecular studies of non-disjunction in trisomy 16.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682425

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

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682425

Distribution of aneuploidy in human gametes: comparison between human sperm and oocytes.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682425

Trisomy 21: association between reduced recombination and 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=1682425

Molecular, cytogenetic, and clinical investigations of Prader-Willi syndrome patients

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682425

Uniparental paternal disomy in Angelman's 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=1682425

The frequency of uniparental disomy in Prader-Willi syndrome. Implications for molecular diagnosis.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682425

Third International Workshop on 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=1682425

Paternal uniparental disomy of chromosome 15 in a child with Angelman 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=1682425

A mapping function for man

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682425

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

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682425

Deletion breakpoints associated with the Prader-Willi and Angelman syndromes (15q11-q13) are not sites of high homologous recombination

15 November 2018

1 reference

12 December 2020

Origin of teratomas and twins

1 reference

12 December 2020

Reduced recombination rate on chromosomes 21 that have undergone nondisjunction

1 reference

12 December 2020

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

1 reference

12 December 2020

Multilocus recombination frequencies

1 reference

12 December 2020

The CEPH consortium linkage map of human chromosome 15q

1 reference

12 December 2020

A new genetic concept: uniparental disomy and its potential effect, isodisomy

1 reference

12 December 2020

Reduced recombination and paternal age effect in Klinefelter syndrome

1 reference

12 December 2020

Tests of hypotheses on recombination frequencies

1 reference

12 December 2020

Gene-centromere mapping and the study of non-disjunction in autosomal trisomies and ovarian teratomas

1 reference

12 December 2020

Identifiers

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8352279%20AND%20SRC:MED&resulttype=core&format=json

30 October 2019

PubMed publication ID

8352279

1 reference