Donor age and the frequency of disomy for chromosomes 1, 13, 21 and structural abnormalities in human spermatozoa using multicolour fluorescence in-situ hybridization

Human Reproduction

Volumn 13, Issue 9, 1998, Pages 2489-2494

  McInnes, Brenda ^a,b   Rademaker, Alfred ^c   Martin, Renée ^a,b  

^a UNIVERSITY OF CALGARY   (Canada)

^b ALBERTA CHILDREN'S HOSPITAL   (Canada)

^c NORTHWESTERN UNIVERSITY   (United States)

Author keywords

Age; Aneuploidy; FISH; Spermatozoa

Indexed keywords

ADULT; ANEUPLOIDY; ARTICLE; CELL STRUCTURE; CHROMOSOME 1; CHROMOSOME 13; CHROMOSOME 21; CHROMOSOME ABERRATION; CHROMOSOME DELETION; CHROMOSOME DUPLICATION; DISOMY; DNA PROBE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; HUMAN CELL; LIVING DONOR; MALE; NORMAL HUMAN; SPERMATOZOON;

EID: 0031655766     PISSN: 02681161     EISSN: None     Source Type: Journal    
DOI: 10.1093/humrep/13.9.2489     Document Type: Article

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