Characterization of a 8q21.11 Microdeletion Syndrome Associated with Intellectual Disability and a Recognizable Phenotype-Reference-Cited by-同舟云学术

Characterization of a 8q21.11 Microdeletion Syndrome Associated with Intellectual Disability and a Recognizable Phenotype

Published:2011-08 Issue:2 Volume:89 Page:295-301
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Palomares María,Delicado Alicia,Mansilla Elena,de Torres María Luisa,Vallespín Elena,Fernandez Luis,Martinez-Glez Victor,García-Miñaur Sixto,Nevado Julián,Simarro Fernando Santos,Ruiz-Perez Victor L.,Lynch Sally Ann,Sharkey Freddie H.,Thuresson Ann-Charlotte,Annerén Göran,Belligni Elga F.,Martínez-Fernández María Luisa,Bermejo Eva,Nowakowska Beata,Kutkowska-Kazmierczak Anna,Bocian Ewa,Obersztyn Ewa,Martínez-Frías María Luisa,Hennekam Raoul C.M.,Lapunzina Pablo

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference14 articles.

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4. Application of metaphase HR-CGH and targeted Chromosomal Microarray Analyses to genomic characterization of 116 patients with mental retardation and dysmorphic features;Nowakowska;Am. J. Med. Genet. A.,2008

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