The association of split hand foot malformation (SHFM) and congenital heart defects
Author:
Publisher
Wiley
Subject
Developmental Biology,Embryology,General Medicine,Pediatrics, Perinatology, and Child Health
Reference95 articles.
1. X-Chromosomally inherited split-hand/split-foot anomaly in a Pakistani kindred
2. Proximal chromosome 8q deletion in a boy with femoral bifurcation and other multiple congenital anomalies
3. Apparently new oculo-cerebro-acral syndrome
4. A new locus for split hand/foot malformation with long bone deficiency (SHFLD) at 2q14.2 identified from a chromosome translocation
5. Wolf-Hirschhorn syndrome and a split-hand malformation
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1. Split-Hand/Foot Malformation (SHFM);Genetic Syndromes;2024
2. Identification of a novel heterozygous missense TP63 variant in a Chinese pedigree with split-hand/foot malformation;BMC Medical Genomics;2022-07-13
3. A novel chromosome 2q24.3‐q32.1 microdeletion in a fetus with multiple malformations;Journal of Clinical Laboratory Analysis;2022-07-12
4. Sequence Variants in the WNT10B and TP63 Genes Underlying Isolated Split-Hand/Split-Foot Malformation;Genetic Testing and Molecular Biomarkers;2020-09-01
5. A Novel Homozygous Nonsense Mutation p.Cys366* in the WNT10B Gene Underlying Split-Hand/Split Foot Malformation in a Consanguineous Pakistani Family;Frontiers in Pediatrics;2020-01-09
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