Exome sequencing reveals a heterozygous DLX5 mutation in a Chinese family with autosomal-dominant split-hand/foot malformation

BMP-Mediated Functional Cooperation between Dlx5;Dlx6 and Msx1;Msx2 during Mammalian Limb Development

(2013) Maxence Vieux-Rochas et al.   PLoS One

A 0.7 Mb de novo duplication at 7q21.3 including the genesDLX5andDLX6in a patient with split-hand/split-foot malformation

(2012) Milen Velinov et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

A novel homozygous missense mutation in WNT10B in familial split-hand/foot malformation

(2011) S Khan et al.   CLINICAL GENETICS

Identification of a novelDLX5mutation in a family with autosomal recessive split hand and foot malformation

(2011) Hanan E Shamseldin et al.   JOURNAL OF MEDICAL GENETICS

A method and server for predicting damaging missense mutations

(2010) Ivan A Adzhubei et al.   NATURE METHODS

Comprehensive expression analysis of all Wnt genes and their major secreted antagonists during mouse limb development and cartilage differentiation

(2009) Florian Witte et al.   GENE EXPRESSION PATTERNS

DLX5(Distal-less Homeobox 5) Promotes Tumor Cell Proliferation by Transcriptionally RegulatingMYC

(2009) Jinfei Xu et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

P-cadherin is a p63 target gene with a crucial role in the developing human limb bud and hair follicle

(2008) Y. Shimomura et al.   DEVELOPMENT

Homozygous WNT10b mutation and complex inheritance in Split-Hand/Foot Malformation

(2008) Sibel Aylin Ugur et al.   HUMAN MOLECULAR GENETICS