Literature DB >> 10649803

A 68-year-old white female with Prader-Willi syndrome.

M G Butler.   

Abstract

A 68-year-old white female with Prader-Willi syndrome is described. The clinical features are described and the progression of her condition is discussed and illustrated.

Entities:  

Mesh：

Year:  2000        PMID： 10649803      PMCID： PMC5233433          DOI： 10.1097/00019605-200009010-00015

Source DB:  PubMed          Journal:  Clin Dysmorphol        ISSN： 0962-8827            Impact factor:   0.816


  6 in total

1.  Genetic imprinting suggested by maternal heterodisomy in nondeletion Prader-Willi syndrome.

Authors:  R D Nicholls; J H Knoll; M G Butler; S Karam; M Lalande
Journal:  Nature       Date:  1989-11-16       Impact factor: 49.962

2.  The frequency of uniparental disomy in Prader-Willi syndrome. Implications for molecular diagnosis.

Authors:  M J Mascari; W Gottlieb; P K Rogan; M G Butler; D A Waller; J A Armour; A J Jeffreys; R L Ladda; R D Nicholls
Journal:  N Engl J Med       Date:  1992-06-11       Impact factor: 91.245

Review 3.  Prader-Willi syndrome.

Authors:  S B Cassidy
Journal:  Curr Probl Pediatr       Date:  1984-01

4.  Prader-Willi Syndrome: Genetics and Behavior.

Authors:  Travis Thompson; Merlin G Butler; William E MacLean; Beth Joseph
Journal:  Peabody J Educ       Date:  1996

Review 5.  Imprinting in Prader-Willi and Angelman syndromes.

Authors:  R D Nicholls; S Saitoh; B Horsthemke
Journal:  Trends Genet       Date:  1998-05       Impact factor: 11.639

6.  Prader-Willi syndrome: current understanding of cause and diagnosis.

Authors:  M G Butler
Journal:  Am J Med Genet       Date:  1990-03
  6 in total
  1 in total

1.  Prader-Willi Syndrome: Clinical and Genetic Findings.

Authors:  Merlin G Butler; Travis Thompson
Journal:  Endocrinologist       Date:  2000-07
  1 in total

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