3q29 Microdeletion Syndrome: Clinical and Molecular Characterization of a New Syndrome-Reference-Cited by-同舟云学术

3q29 Microdeletion Syndrome: Clinical and Molecular Characterization of a New Syndrome

Published:2005-07 Issue:1 Volume:77 Page:154-160
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Willatt Lionel,Cox James,Barber John,Cabanas Elisabet Dachs,Collins Amanda,Donnai Dian,FitzPatrick David R.,Maher Eddy,Martin Howard,Parnau Josep,Pindar Lesley,Ramsay Jacqueline,Shaw-Smith Charles,Sistermans Erik A.,Tettenborn Michael,Trump Dorothy,de Vries Bert B.A.,Walker Kate,Raymond F. Lucy

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference20 articles.

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2. PAK3 mutation in nonsyndromic X-linked mental retardation;Allen;Nat Genet,1998

3. Telomeres: a diagnosis at the end of the chromosomes;De Vries;J Med Genet,2003

4. Hemizygosity at the elastin locus in a developmental disorder, Williams syndrome;Ewart;Nat Genet,1993

5. The use of telomere probes to investigate submicroscopic rearrangements associated with mental retardation;Flint;Curr Opin Genet Dev,2003

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