Split hand/foot malformation syndrome (SHFM): rare congenital orthopaedic disorder-Reference-Cited by-同舟云学术

Split hand/foot malformation syndrome (SHFM): rare congenital orthopaedic disorder

Published:2014-06-27 Issue:jun27 1 Volume:2014 Page:bcr2014204731-bcr2014204731
ISSN:1757-790X
Container-title:Case Reports
language:en
Short-container-title:Case Reports

Author:

Patel A.,Sharma D.,Yadav J.,Garg E.

Publisher

BMJ

Subject

General Medicine

Reference11 articles.

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4. Kay SP, McCombe D. Central hand deficiences. In: Green DP, Pederson MD, Hotchkiss RN, Wolf SW, eds. Green's Operative Hand Surgery. 5th ed. Philadelphia: Elsevier Churchill Livingstone, 2005:1404–15.

5. The p63 gene in EEC and other syndromes;Brunner;J Med Genet,2002

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1. Identification of a novel heterozygous missense TP63 variant in a Chinese pedigree with split-hand/foot malformation;BMC Medical Genomics;2022-07-13

2. Whole genome sequencing reveals translocation breakpoints disrupting TP63 gene underlying split hand/foot malformation in a Chinese family;Molecular Genetics & Genomic Medicine;2021-01-20

3. P63 modulates the expression of the WDFY2 gene which is implicated in cancer regulation and limb development;Bioscience Reports;2019-12

4. Ectrodactyly, Ectodermal Dysplasia, Cleft Lip, and Palate (EEC Syndrome) with Tetralogy of Fallot: A Very Rare Combination;Frontiers in Pediatrics;2015-06-16