Annals of Child Neurology

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Split-Hand/Foot Malformation and Subependymal Heterotopia Caused by a DLX5 Gene Mutation: A Case Report

Jun Hee Shin, Min Jeong Han, Sun Jun Kim

Ann Child Neurol. 2021;29(4):199-201. Published online August 25, 2021
DOI: https://doi.org/10.26815/acn.2021.00472

Split-Hand/Foot Malformation and Subependymal Heterotopia Caused by a DLX5 Gene Mutation: A Case Report

Jun Hee Shin, Min Jeong Han, Sun Jun Kim

Annals of Child Neurology. 2021;29(4):199-201

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Split hand foot malformation is associated with a reduced level of Dactylin gene expression

D Basel, A DePaepe, MW Kilpatrick, P Tsipouras

Clinical Genetics. 2003;64(4):350-354

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Split hand foot malformation: Presentation of a rare case and description of a novel technique in management of split hand Study design: Case report

Odisha Journal of Orthopaedics and Trauma. 2020;41(1):

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Split Hand Foot Malformation (SHFM)

AM Elliott, JA Evans, AE Chudley

Clinical Genetics. 2005;68(6):501-505

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Split-hand/split-foot malformation with paternal mutation in the p63 gene

Ingrid Witters, Hans Van Bokhoven, A. Goossens, Frans-Andr� Van Assche, Jean-Pierre Fryns

Prenatal Diagnosis. 2001;21(13):1119-1122

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Split Hand/Foot Malformation

Diagnostic Imaging: Obstetrics. 2016;754-757

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Anorectal malformation associated with a mutation in the P63 gene in a family with split hand–foot malformation

Pengjun Su, Yuhang Yuan, Ying Huang, Weilin Wang, Zhibo Zhang

International Journal of Colorectal Disease. 2013;28(12):1621-1627

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Split-Hand/Split-Foot Malformation Is Caused by Mutations in the p63 Gene on 3q27

Peter Ianakiev, Michael W. Kilpatrick, Iva Toudjarska, Donald Basel, Peter Beighton, Petros Tsipouras

The American Journal of Human Genetics. 2000;67(1):59-66

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Split hand/foot malformation with long bone deficiency associated with BHLHA9 gene duplication: a case report and review of literature

Chamara Sampath Paththinige, Nirmala Dushyanthi Sirisena, Fabienne Escande, Sylvie Manouvrier, Florence Petit, Vajira Harshadeva Weerabaddana Dissanayake

BMC Medical Genetics. 2019;20(1):

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Split hand/split foot malformation with hearing loss: first report of families linked to the SHFM1 locus in 7q21

D Tackels-Horne, A Toburen, E Sangiorgi, F Gurrieri, X De Mollerat, R Fischetto, F Causio, K Clarkson, Re Stevenson, Ce Schwartz

Clinical Genetics. 2001;59(1):28-36

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