Centromeric genotyping and direct analysis of nondisjunction in humans: Down syndrome

Chromosoma

Volumn 107, Issue 3, 1998, Pages 166-172

  Shen, J J ^a   Sherman, S L ^a,b   Hassold, Terry J ^a  

^a UNIVERSITY HOSPITALS OF CLEVELAND   (United States)

^b EMORY UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CENTROMERE; CHROMOSOME CHIASM; CLINICAL ARTICLE; DOWN SYNDROME; GENE MAPPING; GENETIC RECOMBINATION; GENOTYPE; HUMAN; HUMAN CELL; HYBRID CELL; MEIOSIS; NONDISJUNCTION; TRISOMY 21;

CENTROMERE; CHROMOSOMES, HUMAN, PAIR 21; DOWN SYNDROME; ELECTROPHORESIS, GEL, PULSED-FIELD; FAMILY HEALTH; FEMALE; GENETIC MARKERS; GENOTYPE; HUMANS; HYBRID CELLS; MALE; MEIOSIS; MOTHERS; NONDISJUNCTION, GENETIC; RECOMBINATION, GENETIC; TRISOMY;

EID: 0031926521     PISSN: 00095915     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004120050293     Document Type: Article

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