2q24–q31 Deletion: Report of a case and review of the literature-Reference-Cited by-同舟云学术

2q24–q31 Deletion: Report of a case and review of the literature

Published:2007-01 Issue:1 Volume:50 Page:21-32
ISSN:1769-7212
Container-title:European Journal of Medical Genetics
language:en
Short-container-title:European Journal of Medical Genetics

Author:

Pescucci C.,Caselli R.,Grosso S.,Mencarelli M.A.,Mari F.,Farnetani M.A.,Piccini B.,Artuso R.,Bruttini M.,Priolo M.,Zuffardi O.,Gimelli S.,Balestri P.,Renieri A.

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics,General Medicine

Reference31 articles.

1. Interneuron migration from basal forebrain to neocortex: dependence on Dlx genes;Anderson;Science,1997

2. Real-time quantitative PCR as a routine method for screening large rearrangements in Rett syndrome: report of one case of MECP2 deletion and one case of MECP2 duplication;Ariani;Hum. Mutat.,2004

3. A second locus for familial generalized epilepsy with febrile seizures plus maps to chromosome 2q21–q33;Baulac;Am. J. Hum. Genet.,1999

4. Interstitial deletion 2q24.3: case report with high resolution banding;Bernar;J. Med. Genet.,1985

5. Increased nuchal translucency and split-hand/foot malformation in a fetus with an interstitial deletion of chromosome 2q that removes the SHFM5 locus;Bijlsma;Prenat. Diagn.,2005

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