Clinical and genetic findings in Hungarian pediatric patients carrying chromosome 16p copy number variants and a review of the literature-Reference-Cited by-同舟云学术

Clinical and genetic findings in Hungarian pediatric patients carrying chromosome 16p copy number variants and a review of the literature

Published:2020-10 Issue:10 Volume:63 Page:104027
ISSN:1769-7212
Container-title:European Journal of Medical Genetics
language:en
Short-container-title:European Journal of Medical Genetics

Author:

Lengyel Anna,Pinti Éva,Pikó Henriett,Jávorszky Eszter,David Dezső,Tihanyi Mariann,Gönczi Éva,Kiss Eszter,Tóth Zsuzsa,Tory Kálmán,Fekete György,Haltrich Irén

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics,General Medicine

Reference72 articles.

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2. A large and complex structural polymorphism at 16p12.1 underlies microdeletion disease risk;Antonacci;Nat. Genet.,2010

3. Recurrent 200-kb deletions of 16p11.2 that include the SH2B1 gene are associated with developmental delay and obesity;Bachmann-Gagescu;Genet. Med.,2010

4. The atypical 16p11.2 deletion: a not so atypical microdeletion syndrome?;Barge-Schaapveld;Am. J. Med. Genet.,2011

5. Further characterization of the new microdeletion syndrome of 16p11.2-p12.2;Battaglia;Am. J. Med. Genet.,2009

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