Evidence for an additional locus for split hand/foot malformation in chromosome region 8q21.11–q22.3
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Reference17 articles.
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1. Diagnostic yield of exome sequencing in congenital vertical talus;European Journal of Medical Genetics;2022-06
2. Sequence Variants in the WNT10B and TP63 Genes Underlying Isolated Split-Hand/Split-Foot Malformation;Genetic Testing and Molecular Biomarkers;2020-09-01
3. Nonsyndromic Split-Hand/Foot Malformation: Recent Classification;Molecular Syndromology;2019
4. First direct evidence of involvement of a homozygous loss-of-function variant in the EPS15L1 gene underlying split-hand/split-foot malformation;Clinical Genetics;2018-01-25
5. Homozygous sequence variants in the WNT10B gene underlie split hand/foot malformation;Genetics and Molecular Biology;2018-01-22
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