Associated Papers
Feeding difficulty is the dominant feature in 12 Chinese newborns with CHD7 pathogenic variants.
Chen X et al.
Bmc Medical Genetics, 2019
31146700 (PubMed )
Supplement: 12881_2019_813_MOESM1_ESM.xls › CHD7_ChenXiang_query_Report_Fil
A Novel Homozygous Nonsense Mutation p.Cys366* in the WNT10B Gene Underlying Split-Hand/Split Foot Malformation in a Consanguineous Pakistani Family.
Khan A et al.
Frontiers in Pediatrics, 2019
Mutations in WNT10B Are Identified in Individuals with Oligodontia.
Yu P et al.
American Journal of Human Genetics, 2016
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