(Q36723618)

English

A fluorescent in situ hybridization analysis of X chromosome pairing in early human female meiosis

scientific article published on October 1994

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

15 August 2017

A fluorescent in situ hybridization analysis of X chromosome pairing in early human female meiosis (English)

1 reference

Europe PubMed Central

PubMed publication ID

15 August 2017

author name string

Y E Cheng

1

1 reference

Europe PubMed Central

PubMed publication ID

15 August 2017

S M Gartler

2

1 reference

Europe PubMed Central

PubMed publication ID

15 August 2017

publication date

1 October 1994

1 reference

Europe PubMed Central

PubMed publication ID

15 August 2017

1 reference

Europe PubMed Central

PubMed publication ID

15 August 2017

94

1 reference

Europe PubMed Central

PubMed publication ID

15 August 2017

4

1 reference

Europe PubMed Central

PubMed publication ID

15 August 2017

389-394

1 reference

Europe PubMed Central

PubMed publication ID

15 August 2017

Asymmetry in chromosome pairing: a major factor in de novo mutation and the production of genetic disease in man

1 reference

https://pubmed.ncbi.nlm.nih.gov/7927335

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/7927335

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/7927335

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

1 reference

https://pubmed.ncbi.nlm.nih.gov/7927335

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

OOCYTES IN PROPHASE OF MEIOSIS FROM SQUASH PREPARATIONS OF HUMAN FETAL OVARIES

1 reference

https://pubmed.ncbi.nlm.nih.gov/7927335

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosome in situ suppression hybridisation in human male meiosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/7927335

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fluorescence in situ hybridization with human chromosome-specific libraries: detection of trisomy 21 and translocations of chromosome 4.

1 reference

https://pubmed.ncbi.nlm.nih.gov/7927335

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Trisomy 21: association between reduced recombination and nondisjunction

1 reference

https://pubmed.ncbi.nlm.nih.gov/7927335

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chiasma frequency and maternal age in mammals.

1 reference

https://pubmed.ncbi.nlm.nih.gov/7927335

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/7927335

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/7927335

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Development of the first meiotic prophase stages in human fetal oocytes observed by light and electron microscopy

1 reference

https://pubmed.ncbi.nlm.nih.gov/7927335

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Meiotic chromosome pairing in the normal human female.

1 reference

https://pubmed.ncbi.nlm.nih.gov/7927335

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/7927335

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular studies of non-disjunction in trisomy 16.

1 reference

https://pubmed.ncbi.nlm.nih.gov/7927335

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Frequency and distribution of aneuploidy in human female gametes.

1 reference

https://pubmed.ncbi.nlm.nih.gov/7927335

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Trisomy 21 (Down syndrome): studying nondisjunction and meiotic recombination by using cytogenetic and molecular polymorphisms that span chromosome 21.

1 reference

https://pubmed.ncbi.nlm.nih.gov/7927335

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosomal analysis of unfertilized human oocytes prepared by a gradual fixation-air drying method

1 reference

https://pubmed.ncbi.nlm.nih.gov/7927335

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular studies of trisomy 18

1 reference

https://pubmed.ncbi.nlm.nih.gov/7927335

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Oocyte selection: a new model for the maternal-age dependence of Down syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/7927335

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The prophase stages in human foetal oocytes studied by light and electron microscopy

1 reference

https://pubmed.ncbi.nlm.nih.gov/7927335

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

OBSERVATIONS ON THE MOVEMENTS OF THE LIVING PRIMORDIAL GERM CELLS IN THE MOUSE

1 reference

https://pubmed.ncbi.nlm.nih.gov/7927335

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00201599

1 reference

Europe PubMed Central

PubMed publication ID

15 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

15 August 2017

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