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Article

Sequence Variants in the WNT10B and TP63 Genes Underlying Isolated Split-Hand/Split-Foot Malformation.

Genetic testing and molecular biomarkers - 1 Sept 2020

Bilal Muhammad, Hayat Amir, Umair Muhammad, Ullah Asmat, Khawaja Sundus, Malik Erum, Burmeister Margit, Bibi Nousheen, Umm-E-Kalsoom, Memon Muhammad Iqbal, Basit Sulman, Ahmad Wasim, Khan Bushra

Abstract excerpt

Aims: Split-hand/split-foot malformation (SHFM) is a developmental and congenital limb malformation characterized by variable degrees of medial clefting or absence of one or more digits in hands and/or feet. The aim of this study was to identify the underlying cause of three consanguineous Pakistani families showing various types of SHFM-related features. Materials and Methods: Standard molecular methods,...

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PMID: 32762550
DOI: 10.1089/gtmb.2020.0024

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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