Detection of aberrant DNA methylation in unique Prader — Willi syndrome patients and its diagnostic implications-Reference-Cited by-同舟云学术

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Detection of aberrant DNA methylation in unique Prader — Willi syndrome patients and its diagnostic implications

Published:1994 Issue:6 Volume:3 Page:893-895
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Hum Mol Genet

Author:

Buiting Karin,Dittrich Bärbel,Robinson Wendy P.,Guitart Mirlam,Abeliovich Dvorah,Lerer Israela,Horsthemke Bernhard

Publisher

Oxford University Press (OUP)

Subject

Genetics(clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/3/6/893/1608236/3-6-893.pdf

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2. The role of imprinted genes in humans;Molecular Aspects of Medicine;2013-07

3. Prader-Willi syndrome and Angelman syndrome;American Journal of Medical Genetics Part C: Seminars in Medical Genetics;2010-08-20

4. Clinical features and molecular genetic analysis of a boy with Prader-Willi syndrome caused by an imprinting defect;Acta Paediatrica;2008-01-21

5. Hyperphagic short stature and Prader–Willi syndrome: A comparison of behavioural phenotypes, genotypes and indices of stress;British Journal of Psychiatry;2001-08

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