A clinical, cytogenetic, and molecular study of 40 adults with the Prader-Willi syndrome.

Author:

Webb T,Clarke D,Hardy C A,Kilpatrick M W,Corbett J,Dahlitz M

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference31 articles.

1. Ein Syndrom von Adipositas, Kleinwuchs, Kryptorchismus und Oligophrenic nach Myotonicartigem Zustand in Neugeborenalter;Prader, A.; Labhart, A.; Willi, M.;Schweiz Med Wochenschr,1956

2. Clinical and cytogenetic survey of 39 individuals with Prader-Labhart-Willi syndrome;Butler, M.G.; Meaney, F.J.; Palmer, C.G.;Am _7 Med Genet,1986

3. Prader-Willi syndrome (hypotonia, obesity, hypogonadism, growth and mental retardation). J7Ment Defic;Jancar, J.;Res,1971

4. Preventing mental retardation associated with gross obesity in the Prader-Willi syndrome;Crnic, K.A.; Sulzbacher, S.; Snow, J.; Holm, V.A.;Pediatnics,1980

5. Prader-Willi syndrome in a brother and sister without cytogenetic or detectable molecular genetic abnormality at chromosome 15q11q13;Orstavik, K.H.; Tangsrud, S.E.; Kiil, R.;Am J7 Med Genet,1992

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