19q13.32 microdeletion syndrome: Three new cases
Author:
Funder
NICHD
NINDS
Publisher
Elsevier BV
Subject
Genetics (clinical),Genetics,General Medicine
Reference18 articles.
1. Dhx34 and Nbas function in the NMD pathway and are required for embryonic development in zebrafish;Anastasaki;Nucleic Acids Res,2011
2. 2E4/Kaptin (KPTN) – a candidate gene for the hearing loss locus, DFNA4;Bearer;Ann Hum Genet,2000
3. A novel germ cell-specific protein, SHIP1, forms a complex with chromatin remodeling activity during spermatogenesis;Choi;J BiolChem,2008
4. Paternally inherited microdeletion at 15q11.2 confirms a significant role for the SNORD116 C/D box snoRNA cluster in Prader- Willi syndrome;Duker;Eur J Hum Genet,2010
5. Mesodermal Wnt signaling organizes the neural plate via Meis3;Elkouby;Development,2010
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