Associated Papers
Sequence Variants in the WNT10B Underlying Non-Syndromic Split-Hand/Foot Malformation.
Bilal M et al.
Molecular Syndromology, 2023
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
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
Novel homozygous mutations in the WNT10B gene underlying autosomal recessive split hand/foot malformation in three consanguineous families.
Aziz A et al.
Gene, 2014
Homozygous sequence variants in the WNT10B gene underlie split hand/foot malformation.
Ullah A et al.
Genetics and Molecular Biology, 0
Missing Links Between Genetically Inherited Molecules in Split Cord Malformation and Other Anomaly: A Bench to Bedside Approach.
Barik M et al.
Journal of Pediatric Neurosciences, 0
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