Identification of a Novel Variant of ARHGAP29 in a Chinese Family with Nonsyndromic Cleft Lip and Palate.

Jian-Xia TangXiang-Shui XiaoKai WangJie-Yuan JinLiang-Liang Fan Rong Xiang

Published in: BioMed research international (2020)

We detected the disease-causing variant in this NSCL/P family. Our identification expands the genetic spectrum of ARHGAP29 and contributes to novel approaches to the genetic diagnosis and counseling of CL/P families.

Keyphrases

genome wide
bioinformatics analysis
copy number
smoking cessation
gene expression
dna methylation
hiv testing