Chromosome 2p15p16.1 microdeletion syndrome: 2.5 Mb deletion in a patient with renal anomalies, intractable seizures and a choledochal cyst-Reference-Cited by-同舟云学术

Chromosome 2p15p16.1 microdeletion syndrome: 2.5 Mb deletion in a patient with renal anomalies, intractable seizures and a choledochal cyst

Published:2012-08 Issue:8-9 Volume:55 Page:485-489
ISSN:1769-7212
Container-title:European Journal of Medical Genetics
language:en
Short-container-title:European Journal of Medical Genetics

Author:

Hucthagowder Vishwanathan,Liu Ta-Chiang,Paciorkowski Alex R.,Thio Liu Lin,Keller Martin S.,Anderson Christopher D.,Herman Thomas,Dehner Louis P.,Grange Dorothy K.,Kulkarni Shashikant

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics,General Medicine

Reference11 articles.

1. Singleton deletions throughout the genome increase risk of bipolar disorder;Zhang;Mol. Psychiatry,2009

2. Further characterization of microdeletion syndrome involving 2p15-p16.1;Felix;Am. J. Med. Genet. A,2010

3. Clinical and molecular cytogenetic characterisation of a newly recognised microdeletion syndrome involving 2p15-16.1;Rajcan-Separovic;J. Med. Genet.,2007

4. The facial dysmorphy in the newly recognised microdeletion 2p15-p16.1 refined to a 570 kb region in 2p15;Chabchoub;J. Med. Genet.,2008

5. A newly recognised microdeletion syndrome involving 2p15p16.1: narrowing down the critical region by adding another patient detected by genome wide tiling path array comparative genomic hybridisation analysis;de Leeuw;J. Med. Genet.,2008

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