Microduplication 22q11.2, an Emerging Syndrome: Clinical, Cytogenetic, and Molecular Analysis of Thirteen Patients-Reference-Cited by-同舟云学术

Microduplication 22q11.2, an Emerging Syndrome: Clinical, Cytogenetic, and Molecular Analysis of Thirteen Patients

Published:2003-11 Issue:5 Volume:73 Page:1027-1040
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Ensenauer Regina E.,Adeyinka Adewale,Flynn Heather C.,Michels Virginia V.,Lindor Noralane M.,Dawson D. Brian,Thorland Erik C.,Lorentz Cindy Pham,Goldstein Jennifer L.,McDonald Marie T.,Smith Wendy E.,Simon-Fayard Elba,Alexander Alan A.,Kulharya Anita S.,Ketterling Rhett P.,Clark Robin D.,Jalal Syed M.

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference31 articles.

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3. Two autosomal dominant neuropathies result from reciprocal DNA duplication deletion of a region on chromosome 17;Chance;Hum Mol Genet,1994

4. The organization of the γ-glutamyl transferase genes and other low copy repeats in human chromosome 22q11;Collins;Genome Res,1997

5. DNA fluorescent probes for diagnosis of velocardiofacial and related syndromes;Crifasi;Mayo Clin Proc,1995

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