A small de novo 16q24.1 duplication in a woman with severe clinical features-Reference-Cited by-同舟云学术

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A small de novo 16q24.1 duplication in a woman with severe clinical features

Published:2013-04 Issue:4 Volume:56 Page:211-215
ISSN:1769-7212
Container-title:European Journal of Medical Genetics
language:en
Short-container-title:European Journal of Medical Genetics

Author:

Quéméner-Redon Sylvia,Bénech Caroline,Audebert-Bellanger Séverine,Friocourt Gaëlle,Planes Marc,Parent Philippe,Férec Claude

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics,General Medicine

Reference23 articles.

1. Diagnostic investigations in individuals with mental retardation: a systematic literature review of their usefulness;Van Karnebeek;Eur. J. Hum. Genet.,2005

2. Diagnostic yield of various genetic approaches in patients with unexplained developmental delay or mental retardation;Rauch;Am. J. Med. Genet. A,2006

3. Use of array CGH in the evaluation of dysmorphology, malformations, developmental delay, and idiopathic mental retardation;Stankiewicz;Curr. Opin. Genet. Dev.,2007

4. Molecular characterization of partial trisomy 16q24.1-qter: clinical report and review of the literature;Brisset;Am. J. Med. Genet.,2002

5. Trisomy 16q arising from a maternal 15p;16q translocation;Ridler;J. Med. Genet.,1979

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3. Identification of an elaborate complex mediating postsynaptic inhibition;Science;2016-09-09

4. Prenatal diagnosis and molecular cytogenetic characterization of de novo partial monosomy 3p (3p26.3→pter) and partial trisomy 16q (16q23.1→qter);Taiwanese Journal of Obstetrics and Gynecology;2016-04

5. The Molecular Convergence of Birdsong and Speech;Animal Models of Speech and Language Disorders;2013

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