New insights into human nondisjunction of chromosome 21 in oocytes

PLoS Genetics

Volumn 4, Issue 3, 2008, Pages

  Oliver, Tiffany Renee ^a   Feingold, Eleanor ^b   Yu, Kai ^c   Cheung, Vivian ^d   Tinker, Stuart ^a   Yadav Shah, Maneesha ^a   Masse, Nirupama ^a   Sherman, Stephanie L ^a  

^a EMORY UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b UNIVERSITY OF PITTSBURGH GRADUATE SCHOOL OF PUBLIC HEALTH   (United States)

^c NATIONAL CANCER INSTITUTE   (United States)

^d UNIVERSITY OF PENNSYLVANIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; MICROSATELLITE DNA;

ADULT; ARTICLE; CHROMOSOME 21; DOWN SYNDROME; FEMALE; GENETIC RECOMBINATION; GENOTYPE; HUMAN; INTROSPECTION; MATERNAL AGE; MEIOSIS; MULTIFACTORIAL GENETIC DISORDER; NONDISJUNCTION; OOCYTE; RISK FACTOR; SHORT TANDEM REPEAT; TRISOMY 21; GENETICS; INFANT; MALE; METABOLISM; PREGNANCY;

CHROMOSOMES, HUMAN, PAIR 21; DOWN SYNDROME; FEMALE; HUMANS; INFANT; MALE; MATERNAL AGE; MEIOSIS; MICROSATELLITE REPEATS; NONDISJUNCTION, GENETIC; OOCYTES; PREGNANCY; RECOMBINATION, GENETIC; RISK FACTORS;

EID: 41949097237     PISSN: 15537390     EISSN: 15537404     Source Type: Journal    
DOI: 10.1371/journal.pgen.1000033     Document Type: Article

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