A case with 47, xxy, del(15)(q11;q13) karyotype associated with prader-willi phenotype

Hormone Research in Paediatrics

Volumn 48, Issue 1, 1997, Pages 44-46

  Rego, A ^a   Coll, M D ^b   Regal, M ^a   Guitart, M ^c   Escudero, T ^b   Garcia Mayor R V ^a  

^a HOSPITAL XERAL CÍES   (Spain)

^b UNIVERSITAT AUTÒNOMA DE BARCELONA   (Spain)

^c HOSPITAL CLÍNIC   (Spain)

Author keywords

Fluorescence hybridization analysis; Karyotype; Klinefelter syndrome; Prader Willi syndrome

Indexed keywords

GLUCOSE; TESTOSTERONE;

ANGER; ARTICLE; AUTOMUTILATION; CASE REPORT; CHROMOSOME ANALYSIS; FLUORESCENCE IN SITU HYBRIDIZATION; GLUCOSE BLOOD LEVEL; HUMAN; HYPERGLYCEMIA; HYPERPHAGIA; HYPOPLASIA; KARYOTYPE; KLINEFELTER SYNDROME; MALE; MALE GENITAL TRACT MALFORMATION; MUSCLE HYPOTONIA; OBESITY; PERSONALITY DISORDER; PHENOTYPE; PRADER WILLI SYNDROME; PRIORITY JOURNAL; RESPIRATORY FAILURE; SCHOOL CHILD; SUCKING; TESTOSTERONE BLOOD LEVEL;

EID: 0030954459     PISSN: 16632818     EISSN: 16632826     Source Type: Journal    
DOI: 10.1159/000185422     Document Type: Article

References (5)

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