Khalid Alqosayer
YOU?
Author Swipe
View article: A novel de novo <i>TP63</i> mutation in whole‐exome sequencing of a Syrian family with Oral cleft and ectrodactyly
A novel de novo <i>TP63</i> mutation in whole‐exome sequencing of a Syrian family with Oral cleft and ectrodactyly Open
Background Oral clefts and ectrodactyly are common, heterogeneous birth defects. We performed whole‐exome sequencing (WES) analysis in a Syrian family. The proband presented with both orofacial clefting and ectrodactyly but not ectodermal …
View article: A Novel <i>de novo TP63</i> Mutation in Whole Exome Sequencing of a Syrian Family with Oral Cleft and Ectrodactyly
A Novel <i>de novo TP63</i> Mutation in Whole Exome Sequencing of a Syrian Family with Oral Cleft and Ectrodactyly Open
Oral clefts and ectrodactyly are common, heterogeneous birth defects. We performed whole exome sequencing (WES) analysis in a Syrian family. The proband presented with both orofacial clefting and ectrodactyly. A paternal side second-degree…
View article: Analysis of sequence data to identify potential risk variants for oral clefts in multiplex families
Analysis of sequence data to identify potential risk variants for oral clefts in multiplex families Open
Neither of these candidate genes has previously been associated with oral clefts and, if confirmed as contributing to disease risk, may indicate novel biological pathways in the genetic etiology for oral clefts.