Double aneuploidy (48,XXY,+21): molecular analysis demonstrates a maternal origin

European Journal of Medical Genetics

Volumn 49, Issue 4, 2006, Pages 346-348

  Glass, Ian A ^a   Li, Lei ^b   Cotter, Philip D ^c  

^a UNIVERSITY OF WASHINGTON SCHOOL OF MEDICINE   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

^c CHILDREN S HOSPITAL OAKLAND   (United States)

Author keywords

48,XXY,+21; Double aneuploidy

Indexed keywords

AMNIOCENTESIS; ANEUPLOIDY; CHROMOSOME 21; CHROMOSOME ANALYSIS; CHROMOSOME DISORDER; CYTOGENETICS; GENETIC ANALYSIS; GENETIC PREDISPOSITION; HUMAN; KARYOTYPE; LETTER; TRISOMY; TURNER SYNDROME;

ANEUPLOIDY; CHROMOSOME ABERRATIONS; CHROMOSOMES, HUMAN, PAIR 21; CHROMOSOMES, HUMAN, X; FEMALE; GENETIC TECHNIQUES; HUMANS; MALE; PREGNANCY; SEX CHROMOSOME DISORDERS;

EID: 33745589506     PISSN: 17697212     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ejmg.2005.12.005     Document Type: Letter

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