Publications

Ugur SA et al. Homozygous WNT10B mutation and complex inheritance in Split-Hand/Foot Malformation.Hum Mol Genet. 2008;1;17(17):2644-53. PMID: 18515319.

Aziz A et al. Novel homozygous mutations in the WNT10B gene underlying autosomal recessive split hand/foot malformation in three consanguineous families.Gene. 2014;25;534(2):265-71. PMID: 24211389.

Yu P et al. Mutations in WNT10B are identified in individuals with oligodontia.Am J Hum Genet. 2016;99(1):195-201. PMID: 27321946.

Ullah A et al. Homozygous sequence variants in the WNT10B gene underlie split hand/foot malformation.Genet Mol Biol. 2018;41(1):1-8. PMID: 29384555.

Kantaputra et al. Split hand-foot malformation and a novel WNT10B mutation.Eur J Med Genet. 2018;61(7):372-375. PMID: 29427788.

Kantaputra PN et al. WNT10B mutations associated with isolated dental anomalies.Clin Genet. 2018;93(5):992-999. PMID: 29364501.

Bilal M et al. Sequence Variants in the WNT10B and TP63 Genes Underlying Isolated Split-Hand/Split Foot Malformation.Genet Test Mol Biomarkers. 2020;24(9):600-607. PMID:32762550.

Elalaoui SC et al. Homozygous nonsense mutation of WNT10B gene in a Moroccan family with split-hand foot malformation identified by exome sequencing: a case report. Pan Afr Med J. 2021;39:21. PMID: 34394812.