Trisomy 20 mosaicism in two unrelated girls with skin hypopigmentation and normal intellectual development

American Journal of Medical Genetics

Volumn 99, Issue 3, 2001, Pages 210-216

  Baty, Bonnie J ^a,c   Olson, Susan B ^b   Magenis, R Ellen ^b   Carey, John C ^a  

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

^b OREGON HEALTH AND SCIENCE UNIVERSITY   (United States)

^c UNIVERSITY OF UTAH HEALTH SCIENCES CENTER   (United States)

Author keywords

Hypomelanosis of Ito; Pigmentary dysplasia; Skin hypopigmentation; Trisomy 20 mosaicism

Indexed keywords

AMNIOCENTESIS; AMNION; AMNION CELL; ARTICLE; CASE REPORT; CHILD; CHORION VILLUS; CHROMOSOME MOSAICISM; FEMALE; GENETIC RISK; HUMAN; HYPOMELANOSIS; HYPOPIGMENTATION; INTELLIGENCE; LYMPHOCYTE; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; SKIN FIBROBLAST; TRISOMY 20; URINE SEDIMENT;

CHROMOSOMES, HUMAN, PAIR 20; FEMALE; HUMANS; HYPOPIGMENTATION; INFANT, NEWBORN; INTELLIGENCE; MOSAICISM; PRENATAL DIAGNOSIS; TRISOMY;

EID: 0035869116     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/1096-8628(2001)9999:9999<::AID-AJMG1166>3.0.CO;2-U     Document Type: Article

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