Branchial arch defects and 19p13.12 microdeletion: Defining the critical region into a 0.8 M base interval
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.33908/fullpdf
Reference4 articles.
1. DNA microarray analysis identifies candidate regions and genes in unexplained mental retardation;Engels;Neurology,2007
2. Growth and early postimplantation defects in mice deficient for the bromodomain-containing protein Brd4;Houzelstein;Mol Cell Biol,2002
3. A novel chromosome 19p13.12 deletion in a child with multiple congenital anomalies;Jensen;Am J Med Genet Part A,2009
4. A boy with mental retardation, obesity and hypertrichosis caused by a microdeletion of 19p13.12;Van der Aa;Eur J Med Genet,2010
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2. Confirmation of BRD4 haploinsufficiency role in Cornelia de Lange–like phenotype and delineation of a 19p13.12p13.11 gene contiguous syndrome;Annals of Human Genetics;2018-10-10
3. A recognizable phenotype related to 19p13.12 microdeletion;American Journal of Medical Genetics Part A;2018-07-28
4. First prenatal case of proximal 19p13.12 microdeletion syndrome: New insights and new delineation of the syndrome;European Journal of Medical Genetics;2018-06
5. Reciprocal Relationship between Head Size, an Autism Endophenotype, and Gene Dosage at 19p13.12 Points to AKAP8 and AKAP8L;PLOS ONE;2015-06-15
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