Ovarian dysgenesis in individuals with chromosomal abnormalities (Q46628224)

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scientific article published in April 1991

Language	Label	Description	Also known as
English	Ovarian dysgenesis in individuals with chromosomal abnormalities	scientific article published in April 1991

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

23 December 2017

http://europepmc.org/abstract/MED/2026420

Ovarian dysgenesis in individuals with chromosomal abnormalities (English)

1 reference

Europe PubMed Central

PubMed publication ID

23 December 2017

http://europepmc.org/abstract/MED/2026420

author name string

C Cunniff

1

1 reference

Europe PubMed Central

PubMed publication ID

23 December 2017

http://europepmc.org/abstract/MED/2026420

K L Jones

2

1 reference

Europe PubMed Central

PubMed publication ID

23 December 2017

http://europepmc.org/abstract/MED/2026420

K Benirschke

3

1 reference

Europe PubMed Central

PubMed publication ID

23 December 2017

http://europepmc.org/abstract/MED/2026420

publication date

1 April 1991

1 reference

Europe PubMed Central

PubMed publication ID

23 December 2017

http://europepmc.org/abstract/MED/2026420

1 reference

Europe PubMed Central

PubMed publication ID

23 December 2017

http://europepmc.org/abstract/MED/2026420

86

1 reference

Europe PubMed Central

PubMed publication ID

23 December 2017

http://europepmc.org/abstract/MED/2026420

6

1 reference

Europe PubMed Central

PubMed publication ID

23 December 2017

http://europepmc.org/abstract/MED/2026420

552-556

1 reference

Europe PubMed Central

PubMed publication ID

23 December 2017

http://europepmc.org/abstract/MED/2026420

Follicular development in ovaries of children with Down's syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/2026420

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Oocyte development in XO foetuses of man and mouse: the possible role of heterologous X-chromosome pairing in germ cell survival

1 reference

https://pubmed.ncbi.nlm.nih.gov/2026420

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Meiosis in interspecific equine hybrids. I. The male mule (Equus asinus X E. caballus) and hinny (E. caballus X E. asinus).

1 reference

https://pubmed.ncbi.nlm.nih.gov/2026420

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A reciprocal autosomal translocation which causes male sterility in the mouse also impairs oogenesis.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2026420

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prophase pairing in a mosaic 18p-;iso 18q human female foetus studied by surface spreading

1 reference

https://pubmed.ncbi.nlm.nih.gov/2026420

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Development of the germ cells in the ovary of the mule and hinny

1 reference

https://pubmed.ncbi.nlm.nih.gov/2026420

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Meiotic configurations in female trisomy 21 foetuses

1 reference

https://pubmed.ncbi.nlm.nih.gov/2026420

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Male mule foal qualifies as the offspring of a female mule and jack donkey

1 reference

https://pubmed.ncbi.nlm.nih.gov/2026420

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The ovarian dysgenesis of trisomy 18

1 reference

https://pubmed.ncbi.nlm.nih.gov/2026420

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Reduced oocyte numbers in tertiary trisomic mice with male sterility

1 reference

https://pubmed.ncbi.nlm.nih.gov/2026420

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Triple chromosome synapsis in oocytes from a human foetus with trisomy 21

1 reference

https://pubmed.ncbi.nlm.nih.gov/2026420

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Critical region hypothesis: primary amenorrhea in an 18-year-old woman with a complex translocation (X;2;8).

1 reference

https://pubmed.ncbi.nlm.nih.gov/2026420

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Corpora lutea in proven mules.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2026420

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial premature ovarian failure due to an interstitial deletion of the long arm of the X chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/2026420

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The possible role of meiotic pairing anomalies in the atresia of human fetal oocytes

1 reference

https://pubmed.ncbi.nlm.nih.gov/2026420

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The anatomy and histology of XO human embryos and fetuses

1 reference

https://pubmed.ncbi.nlm.nih.gov/2026420

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A quantitative and cytological study of germ cells in human ovaries

1 reference

https://pubmed.ncbi.nlm.nih.gov/2026420

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fertile mule in China and her unusual foal

1 reference

https://pubmed.ncbi.nlm.nih.gov/2026420

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Oocyte meiosis in a trisomy 18 fetus. Behavior of the supernumerary chromosome and identification of the 18 bivalent

1 reference

https://pubmed.ncbi.nlm.nih.gov/2026420

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Retardation of ovarian growth in male-sterile mice carrying an autosomal translocation

1 reference

https://pubmed.ncbi.nlm.nih.gov/2026420

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ovarian dysgenesis and chromosome abnormalities

1 reference

https://pubmed.ncbi.nlm.nih.gov/2026420

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosomal anomalies that cause male sterility in the mouse also reduce ovary size

1 reference

https://pubmed.ncbi.nlm.nih.gov/2026420

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00201540

1 reference

Europe PubMed Central

PubMed publication ID

23 December 2017

http://europepmc.org/abstract/MED/2026420

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

23 December 2017

http://europepmc.org/abstract/MED/2026420

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