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Prader–Willi and Klinefelter syndrome: a coincidence or not?

  • Published:2007-04 Issue:2 Volume:16 Page:127-129
  • ISSN:0962-8827
  • Container-title:Clinical Dysmorphology
  • language:en
  • Short-container-title:

Author:

Vasudevan Pradeep C.,Quarrell Oliver W.J.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Genetics (clinical),General Medicine,Pathology and Forensic Medicine,Anatomy,Pediatrics, Perinatology and Child Health

Reference15 articles.

1. Klinefelter and trisomy X syndromes in patients with Prader–Willi syndrome and uniparental maternal disomy of chromosome 15: a coincidence?;Butler;Am J Med Genet,1997

2. Prader–Willi syndrome in a child with mosaic trisomy 15 and mosaic triplo-X: a molecular analysis;Devriendt;J Med Genet,1997

3. Prader–Labhart–Willi syndrome with 47, XXX karyotype. Etio-pathogenetic considerations;Ferrante;Minerva Pediatr,1986

4. Oxford desk reference: clinical genetics. 1st ed;Firth,2005

5. Further example of a patient with Prader–Willi and Klinefelter syndromes of different parental origins;Geffroy;Am J Med Genet,1998

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