Analysis of aneuploidy frequencies in sperm from patients with hereditary nonpolyposis colon cancer and an hMSH2 mutation

American Journal of Human Genetics

Volumn 66, Issue 3, 2000, Pages 1149-1152

  Martin, Renee H ^a,b   Green, J ^c   Ko, E ^b   Barclay, L ^b   Rademaker, A W ^d  

^a UNIVERSITY OF CALGARY   (Canada)

^b ALBERTA CHILDREN'S HOSPITAL   (Canada)

^c MEMORIAL UNIVERSITY OF NEWFOUNDLAND   (Canada)

^d NORTHWESTERN UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ANEUPLOIDY; ARTICLE; BASE MISPAIRING; CANADA; CHROMOSOME 13; CHROMOSOME 21; CHROMOSOME SEGREGATION; CLINICAL ARTICLE; COLORECTAL CANCER; CONTROLLED STUDY; DIPLOIDY; DISOMY; EXON; FLUORESCENCE IN SITU HYBRIDIZATION; GENE MUTATION; HETEROZYGOTE; HUMAN; HUMAN CELL; MALE; MEIOSIS; NUCLEIC ACID BASE SUBSTITUTION; PRIORITY JOURNAL; SPERM; X CHROMOSOME; Y CHROMOSOME;

EID: 0033911805     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/302805     Document Type: Article

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