Two cases of maternal uniparental disomy 14 with a phenotype overlapping with the Prader-Willi phenotype [3]

American Journal of Medical Genetics

Volumn 84, Issue 1, 1999, Pages 76-79

  Berends, M J W ^a   Hordijk, R ^a   Scheffer, H ^a   Oosterwijk, J C ^a   Halley, D J J ^a   Sorgedrager, N ^a  

^a UNIVERSITY MEDICAL CENTER GRONINGEN   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

DNA;

CASE REPORT; CHILD; CHROMOSOME ANALYSIS; FEMALE; GENE; HUMAN; LETTER; PHENOTYPE; PHYSICAL EXAMINATION; POLYMERASE CHAIN REACTION; PRADER WILLI SYNDROME; PRIORITY JOURNAL; ROBERTSONIAN CHROMOSOME TRANSLOCATION; UNIPARENTAL DISOMY;

ABNORMALITIES, MULTIPLE; CHILD; CHROMOSOMES, HUMAN, PAIR 14; FEMALE; GENETIC MARKERS; HUMANS; INFANT; KARYOTYPING; MALE; MENTAL RETARDATION; PHENOTYPE; PRADER-WILLI SYNDROME; TRANSLOCATION, GENETIC;

ROBERTSONIA;

EID: 0033531969     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19990507)84:1<76::AID-AJMG16>3.0.CO;2-F     Document Type: Letter

References (13)