Early Prenatal Detection of Recessive Split-hand/Foot Malformation Caused by a Homozygous Variant of WNT10B
Author:
Affiliation:
1. Prenatal Diagnostic Center, Guangzhou Women and Children’s Medical Center Affiliated to Guangzhou Medical University, Guangzhou, Guangdong, China
Publisher
Medknow
Reference6 articles.
1. Genetic regulatory pathways of split-hand/foot malformation;Kantaputra;Clin Genet,2019
2. Evidence for autosomal recessive inheritance of split hand/split foot malformation: A report of nine cases;Gül;Clin Dysmorphol,2002
3. Homozygous nonsense mutation in WNT10B and sporadic split-hand/foot malformation (SHFM) with autosomal recessive inheritance;Blattner;Am J Med Genet A,2010
4. Mutations in WNT10B Are Identified in Individuals with Oligodontia;Yu;Am J Hum Genet,2016
5. Aclassification system for split-hand/foot malformation (SHFM): A proposal based on 3 pedigrees with WNT10B mutations;Al;Eur J Med Genet,2020
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