Mosaicism for deletion 1p36.33 in a Patient with obesity and hyperphagia

American Journal of Medical Genetics

Volumn 70, Issue 4, 1997, Pages 409-412

  Eugster, Erica A ^a   Berry, Susan A ^a   Hirsch, Betsy ^a,b  

^a UNIVERSITY OF MINNESOTA MEDICAL SCHOOL   (United States)

^b UNIVERSITY OF MINNESOTA   (United States)

Author keywords

1p36.3 deletion; Hyperphagia; Mosaicism; Obesity; Prader Willi syndrome

Indexed keywords

ARTICLE; CASE REPORT; CHILD; CHROMOSOME 1P; CHROMOSOME MOSAICISM; CYTOGENETICS; DISEASE ASSOCIATION; FEMALE; GENE DELETION; GENETIC ANALYSIS; HUMAN; HYPERPHAGIA; INCIDENCE; OBESITY; PHENOTYPE; PRADER WILLI SYNDROME; PRIORITY JOURNAL;

CHILD, PRESCHOOL; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 1; FEMALE; HUMANS; HYPERPHAGIA; MONOSOMY; MOSAICISM; OBESITY;

EID: 0030958923     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19970627)70:4<409::AID-AJMG14>3.0.CO;2-L     Document Type: Article

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