Molecular Analysis of Twelve Pakistani Families with Nonsyndromic or Syndromic Hearing Loss

Por Wang, Rongrong, Han, Shirui, Khan, Amjad, Zhang, Xue
Publicado no Genet Test Mol Biomarkers (2017)

A novel homozygous missense mutation in BHLHA9 causes mesoaxial synostotic syndactyly with phalangeal reduction in a Pakistani family

Por Khan, Amjad, Wang, Rongrong, Han, Shirui, Ahmad, Wasim, Zhang, Xue
Publicado no Hum Genome Var (2017)

Clinical and genetic characteristics of Chinese patients with familial or sporadic pediatric cataract

Por Li, Jingyan, Leng, Yunji, Han, Shirui, Yan, Lulu, Lu, Chaoxia, Luo, Yang, Zhang, Xue, Cao, Lihua
Publicado no Orphanet J Rare Dis (2018)