Comparison of high resolution cytogenetics, fluorescence in situ hybridisation, and DNA studies to validate the diagnosis of Prader-Willi and Angelman's syndromes.-Reference-Cited by-同舟云学术

Comparison of high resolution cytogenetics, fluorescence in situ hybridisation, and DNA studies to validate the diagnosis of Prader-Willi and Angelman's syndromes.

Published:1995-05-01 Issue:5 Volume:72 Page:397-402
ISSN:0003-9888
Container-title:Archives of Disease in Childhood
language:en
Short-container-title:Archives of Disease in Childhood

Author:

Smith A,Prasad M,Deng Z M,Robson L,Woodage T,Trent R J

Publisher

BMJ

Subject

Pediatrics, Perinatology and Child Health

Reference40 articles.

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4. Angelman syndrome;Clayton-Smith, J.; Pembrey, M.E.;Jf Med Genet,1992

5. Duplication of chromosome 15 in the region 15ql 1-13 in a patient with developmental delay and ataxia with similarities to Angelman syndrome;Clayton-Smith, J.; Webb, T.; Cheng, X.J.; Pembrey, M.E.; Malcolm, S.;7 Med Genet,1993

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