Literature DB >> 1156680

Familial Prader-Willi syndrome.

E B DeFraites, T F Thurmon, H Farhadian.   

Abstract

Five cases of Prader-Willi syndrome were found in an inbred south Louisiana family. Pedigree data strongly support autosomal recessive inheritance of the syndrome in this family.

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Year:  1975        PMID: 1156680

Source DB:  PubMed          Journal:  Birth Defects Orig Artic Ser        ISSN: 0547-6844


  2 in total

1.  Cytogenetic studies of familial Prader-Willi syndrome.

Authors:  T Hasegawa; M Hara; M Ando; M Osawa; Y Fukuyama; M Takahashi; K Yamada
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

2.  The Prader-Willi syndrome: neuroendocrine study of identical twins.

Authors:  C Trevisan; A Saia; E Schergna; F Mantero
Journal:  Ital J Neurol Sci       Date:  1983-04
  2 in total

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