Associated Papers
Homozygous nonsense mutation of WNT10B gene in a Moroccan family with split-hand foot malformation identified by exome sequencing: a case report.
Elalaoui SC et al.
The Pan African Medical Journal, 2021
Sequence Variants in the WNT10B and TP63 Genes Underlying Isolated Split-Hand/Split-Foot Malformation.
Bilal M et al.
Genetic Testing and Molecular Biomarkers, 2020
WNT10B variants in split hand/foot malformation: Report of three novel families and review of the literature.
Brunelle P et al.
American Journal of Medical Genetics. Part A, 2019
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
Split-hand/foot malformation - molecular cause and implications in genetic counseling.
Sowińska-Seidler A et al.
Journal of Applied Genetics, 2014
Novel homozygous mutations in the WNT10B gene underlying autosomal recessive split hand/foot malformation in three consanguineous families.
Aziz A et al.
Gene, 2014
A novel homozygous missense mutation in WNT10B in familial split-hand/foot malformation.
Khan S et al.
Clinical Genetics, 2012
Homozygous sequence variants in the WNT10B gene underlie split hand/foot malformation.
Ullah A et al.
Genetics and Molecular Biology, 0
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