(Q59549309)

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Investigation of factors associated with paternal nondisjunction of chromosome 21

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scholarly article

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Investigation of factors associated with paternal nondisjunction of chromosome 21 (English)

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Eleanor Feingold

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Eleanor Feingold

3

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author name string

Tiffany Renee Oliver

1

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Archit Bhise

2

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Stuart Tinker

4

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Nirupama Masse

5

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Stephanie L Sherman

6

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language of work or name

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publication date

August 2009

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American Journal of Medical Genetics

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149A

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8

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1685-90

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Excess of males in trisomy 21 (author's transl)

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https://pubmed.ncbi.nlm.nih.gov/19606484

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

New insights into human nondisjunction of chromosome 21 in oocytes

1 reference

https://pubmed.ncbi.nlm.nih.gov/19606484

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/19606484

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Nondisjunction of chromosome 21.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19606484

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Incidence, survival, and mortality in Down syndrome in Denmark.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19606484

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/19606484

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Paternal nondisjunction in trisomy 21: excess of male patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/19606484

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The origin of trisomy in humans.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19606484

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Non-disjunction in human sperm: evidence for an effect of increasing paternal age.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19606484

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Advanced maternal age and the risk of Down syndrome characterized by the meiotic stage of chromosomal error: a population-based study.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19606484

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sex ratios in fetuses and liveborn infants with autosomal aneuploidy.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19606484

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human aneuploidy: incidence, origin, and etiology

1 reference

https://pubmed.ncbi.nlm.nih.gov/19606484

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/19606484

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Estimating meiotic exchange patterns from recombination data: an application to humans

1 reference

https://pubmed.ncbi.nlm.nih.gov/19606484

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization of susceptible chiasma configurations that increase the risk for maternal nondisjunction of chromosome 21

1 reference

https://pubmed.ncbi.nlm.nih.gov/19606484

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Elucidating the mechanisms of paternal non-disjunction of chromosome 21 in humans.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19606484

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Trend analysis of the sex ratio at birth in the United States.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19606484

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

National estimates and race/ethnic-specific variation of selected birth defects in the United States, 1999-2001.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19606484

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The National Down Syndrome Project: design and implementation

1 reference

https://pubmed.ncbi.nlm.nih.gov/19606484

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Polymorphic variation in human meiotic recombination

1 reference

https://pubmed.ncbi.nlm.nih.gov/19606484

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sex ratio in Down syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/19606484

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1002/AJMG.A.32942

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