Aneuploidy in human sperm: the use of multicolor FISH to test various theories of nondisjunction (Q35881410)

10 August 2017

Aneuploidy in human sperm: the use of multicolor FISH to test various theories of nondisjunction (English)

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10 August 2017

Spriggs EL

1

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10 August 2017

Rademaker AW

series ordinal

2

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10 August 2017

Martin RH

series ordinal

3

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10 August 2017

language of work or name

English

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publication date

1 February 1996

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American Journal of Human Genetics

10 August 2017

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10 August 2017

58

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10 August 2017

2

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10 August 2017

356-362

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Molecular studies of trisomy 18

10 August 2017

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914531

Factors affecting the displacement of human chromosomes from the metaphase plate

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914531

Association of ribosomal genes in the fibrillar center of the nucleolus: a factor influencing translocation and nondisjunction in the human meiotic oocyte

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914531

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914531

Trisomy 1 in an eight cell human pre-embryo

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914531

Analysis of DNA haplotypes suggests a genetic predisposition to trisomy 21 associated with DNA sequences on 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=1914531

Macromolecular organization of human centromeric regions reveals high-frequency, polymorphic macro DNA repeats

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914531

Lack of evidence for association of meiotic nondisjunction with particular DNA haplotypes on 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=1914531

Chromosome-specific alpha satellite DNA from the centromere of human chromosome 16

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914531

A human alpha satellite DNA subset specific for chromosome 12

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914531

A cytogenetic and molecular reappraisal of a series of patients with Turner's 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=1914531

Molecular studies of non-disjunction in trisomy 16.

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914531

Frequency and distribution of aneuploidy in human female gametes.

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914531

Identification of two distinct subfamilies of alpha satellite DNA that are highly specific for human chromosome 15.

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914531

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

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914531

XY chromosome nondisjunction in man is associated with diminished recombination in the pseudoautosomal region

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914531

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=1914531

Molecular studies of parental origin and mosaicism in 45,X conceptuses

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914531

Cloning of human satellite III DNA: different components are on different chromosomes

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914531

A Mongol girl with 46 chromosomes

11 July 2018

1 reference

12 December 2020

Direct analysis of the chromosome constitution of human spermatozoa

1 reference

12 December 2020

Nucleolus organizing genes on chromosome 21: recombination and nondisjunction

1 reference

12 December 2020

Further studies on chiasma distribution and interference in the human male

1 reference

12 December 2020

Nucleolar structures in chromosome and SC preparations from human oocytes at first meiotic prophase

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12 December 2020

Reduced recombination and paternal age effect in Klinefelter syndrome

1 reference

12 December 2020

Retrospective study of the parental origin of the extra chromosome in trisomy 18 (Edwards syndrome)

1 reference

12 December 2020

Chromosomal localization of human satellites 2 and 3 by a FISH method using oligonucleotides as probes

1 reference

12 December 2020

Nondisjunction of human acrocentric chromosomes: studies of 432 trisomic fetuses and liveborns

1 reference

12 December 2020

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

1 reference

12 December 2020

Aneuploidy in human sperm: results of two- and three-color fluorescence in situ hybridization using centromeric probes for chromosomes 1, 12, 15, 18, X, and Y

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

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12 December 2020

Identifiers

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10 August 2017

PubMed publication ID

8571962

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