Characterization of a recurrent 15q24 microdeletion syndrome-Reference-Cited by-同舟云学术

Characterization of a recurrent 15q24 microdeletion syndrome

Published:2007-03-01 Issue:5 Volume:16 Page:567-572
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Sharp Andrew J.,Selzer Rebecca R.,Veltman Joris A.,Gimelli Stefania,Gimelli Giorgio,Striano Pasquale,Coppola Antonietta,Regan Regina,Price Sue M.,Knoers Nine V.,Eis Peggy S.,Brunner Han G.,Hennekam Raoul C.,Knight Samantha J.L.,de Vries Bert B.A.,Zuffardi Orsetta,Eichler Evan E.

Publisher

Oxford University Press (OUP)

Subject

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

Link

http://academic.oup.com/hmg/article-pdf/16/5/567/13916519/ddm016.pdf

Reference19 articles.

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2. Discovery of previously unidentified genomic disorders from the duplication architecture of the human genome;Sharp;Nat. Genet.,2006

3. Diagnostic genome profiling in mental retardation;de Vries;Am. J. Hum. Genet.,2005

4. The PML gene is linked to a megabase-scale insertion/deletion restriction fragment length polymorphism;Goy;Genomics,1995

5. Cloning and characterization of a Golgin-related gene from the large-scale polymorphism linked to the PML gene;Gilles;Genomics,2000

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