The 28-kb Deletion Spanning D15S63 Is a Polymorphic Variant in the Ashkenazi Jewish Population-Reference-Cited by-同舟云学术

The 28-kb Deletion Spanning D15S63 Is a Polymorphic Variant in the Ashkenazi Jewish Population

Published:2001-01 Issue:1 Volume:68 Page:261-263
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Silverstein Shira,Lerer Israela,Buiting Karin,Abeliovich Dvorah

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference10 articles.

1. Prader-Willi and Angelman syndromes: diagnostic approach;Abeliovich;J Endocr Genet,2000

2. Diagnostic testing for Prader-Willi and Angleman syndromes: report of the ASHG/ACMG Test and Technology Transfer Committee;American Society of Human Genetics/American College of Medical Genetics Test and Technology Transfer Committee;Am J Hum Genet,1996

3. A 28-kb deletion spanning D15S63 (PW71) in five families: a rare neutral variant?;Buiting;Am J Hum Genet,1999

4. Molecular diagnosis of the Prader-Willi and Angelman syndromes by detection of parent-of-origin specific DNA methylation in 15q11-13;Dittrich;Hum Genet,1992

5. DNA methylation analysis with respect to prenatal diagnosis of the Angelman and Prader-Willi syndromes and imprinting;Glenn;Prenat Diagn,2000

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3. The effect of pedigree structure on detection of deletions and other null alleles;European Journal of Human Genetics;2008-04-16

4. Laboratory Testing for Prader-Willi Syndrome;Management of Prader-Willi Syndrome;2006

5. Detecting Deletions in Families Affected by a Dominant Disease by Use of Marker Data;Human Heredity;2005