Enhanced Maternal Origin of the 22q11.2 Deletion in Velocardiofacial and DiGeorge Syndromes-Reference-Cited by-同舟云学术

Enhanced Maternal Origin of the 22q11.2 Deletion in Velocardiofacial and DiGeorge Syndromes

Published:2013-03 Issue:3 Volume:92 Page:439-447
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Delio Maria,Guo Tingwei,McDonald-McGinn Donna M.,Zackai Elaine,Herman Sean,Kaminetzky Mark,Higgins Anne Marie,Coleman Karlene,Chow Carolyn,Jarlbrzkowski Maria,Bearden Carrie E.,Bailey Alice,Vangkilde Anders,Olsen Line,Olesen Charlotte,Skovby Flemming,Werge Thomas M.,Templin Ludivine,Busa Tiffany,Philip Nicole,Swillen Ann,Vermeesch Joris R.,Devriendt Koen,Schneider Maude,Dahoun Sophie,Eliez Stephan,Schoch Kelly,Hooper Stephen R.,Shashi Vandana,Samanich Joy,Marion Robert,van Amelsvoort Therese,Boot Erik,Klaassen Petra,Duijff Sasja N.,Vorstman Jacob,Yuen Tracy,Silversides Candice,Chow Eva,Bassett Anne,Frisch Amos,Weizman Abraham,Gothelf Doron,Niarchou Maria,van den Bree Marianne,Owen Michael J.,Suñer Damian Heine,Andreo Jordi Rosell,Armando Marco,Vicari Stefano,Digilio Maria Cristina,Auton Adam,Kates Wendy R.,Wang Tao,Shprintzen Robert J.,Emanuel Beverly S.,Morrow Bernice E.

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference44 articles.

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3. A common molecular basis for rearrangement disorders on chromosome 22q11;Edelmann;Hum. Mol. Genet.,1999

4. Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome: Genomic organization and deletion endpoint analysis;Shaikh;Hum. Mol. Genet.,2000

5. Prevalence of 22q11 microdeletion;Tézenas Du Montcel;J. Med. Genet.,1996

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