Sporadic Imprinting Defects in Prader-Willi Syndrome and Angelman Syndrome: Implications for Imprint-Switch Models, Genetic Counseling, and Prenatal Diagnosis-Reference-Cited by-同舟云学术

Sporadic Imprinting Defects in Prader-Willi Syndrome and Angelman Syndrome: Implications for Imprint-Switch Models, Genetic Counseling, and Prenatal Diagnosis

Published:1998-07 Issue:1 Volume:63 Page:170-180
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Buiting Karin,Dittrich Bärbel,Groß Stephanie,Lich Christina,Färber Claudia,Buchholz Tina,Smith Ellie,Reis André,Bürger Joachim,Nöthen Markus M.,Barth-Witte Ulli,Janssen Bart,Abeliovich Dvorah,Lerer Israela,van den Ouweland Ans M.W.,Halley Dicky J.J.,Schrander-Stumpel Connie,Smeets Hubert,Meinecke Peter,Malcolm Sue,Gardner Anne,Lalande Marc,Nicholls Robert D.,Friend Kathie,Schulze Astrid,Matthijs Gert,Kokkonen Hannaleena,Hilbert Pascale,Van Maldergem Lionel,Glover Guillermo,Carbonell Pablo,Willems Patrick,Gillessen-Kaesbach Gabriele,Horsthemke Bernhard

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference50 articles.

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2. A linkage map of human chromosome 15 with an average resolution of 2 cM and containing 55 polymorphic microsatellites;Beckmann;Hum Mol Genet,1993

3. Angelman syndrome in an inbred family;Beuten;Hum Genet,1996

4. Detection of aberrant DNA methylation in unique Prader-Willi syndrome patients and its diagnostic implications;Buiting;Hum Mol Genet,1994

5. Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15;Buiting;Nat Genet,1995

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