Joining the fingers: AHOXD13story

A Switch Between Topological Domains Underlies HoxD Genes Collinearity in Mouse Limbs

(2013) G. Andrey et al.   SCIENCE

Isolated brachydactyly type E caused by a HOXD13 nonsense mutation: a case report

(2012) Aleksander Jamsheer et al.   BMC Medical Genetics

A novel non-synonymous mutation in the homeodomain of HOXD13 causes synpolydactyly in a Chinese family

(2012) Binbin Wang et al.   CLINICA CHIMICA ACTA

Homozygous nonsense mutation in HOXD13 underlies synpolydactyly with a cleft

(2012) Karen J. Low et al.   CLINICAL DYSMORPHOLOGY

Eight-alanine duplication in homeobox D13 in a Chinese family with synpolydactyly

(2012) Qian Xin et al.   GENE

An N-terminal G11A mutation in HOXD13 causes synpolydactyly and interferes with Gli3R function during limb pre-patterning†

(2012) Nathalie Brison et al.   HUMAN MOLECULAR GENETICS

How many entities exist for the spectrum of disorders associated with brachydactyly, syndactyly, short stature, microcephaly, and intellectual disability?

(2011) Aimé Ravel et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Duplication at chromosome 2q31.1-q31.2 in a family presenting syndactyly and nystagmus

(2011) Jamal Ghoumid et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Limb skeletal malformations – What the HOX is going on?

(2011) Nathalie Brison et al.   European Journal of Medical Genetics

A nonsense mutation in the HOXD13 gene underlies synpolydactyly with incomplete penetrance

(2011) Mazen Kurban et al.   JOURNAL OF HUMAN GENETICS

The temporal dynamics of vertebrate limb development, teratogenesis and evolution

(2010) Rolf Zeller   CURRENT OPINION IN GENETICS & DEVELOPMENT

Polyalanine repeat expansion mutation of the HOXD13 gene in a Chinese family with unusual clinical manifestations of synpolydactyly

(2010) Licheng Gong et al.   European Journal of Medical Genetics

Homeobox genes d11–d13 and a13 control mouse autopod cortical bone and joint formation

(2010) Pablo Villavicencio-Lorini et al.   JOURNAL OF CLINICAL INVESTIGATION

2q31.1 microdeletion syndrome: redefining the associated clinical phenotype

(2010) B. Dimitrov et al.   JOURNAL OF MEDICAL GENETICS

A novel microdeletion at chromosome 2q31.1-31.2 in a three-generation family presenting duplication of great toes with clinodactyly

(2009) L-P Tsai et al.   CLINICAL GENETICS

Polyalamine repeat expansion mutations in theHOXD13gene in Pakistani families with synpolydactyly

(2009) M Wajid et al.   CLINICAL GENETICS

Building limb morphology through integration of signalling modules

(2009) Veronique Duboc et al.   CURRENT OPINION IN GENETICS & DEVELOPMENT

The RCAS retroviral expression system in the study of skeletal development

(2009) Christopher T. Gordon et al.   DEVELOPMENTAL DYNAMICS

Genetic screening of 202 individuals with congenital limb malformations and requiring reconstructive surgery

(2009) D Furniss et al.   JOURNAL OF MEDICAL GENETICS

Vertebrate Limb Development: Moving from Classical Morphogen Gradients to an Integrated 4-Dimensional Patterning System

(2009) J.-D. Benazet et al.   Cold Spring Harbor Perspectives in Biology

Identification of aHOXD13mutation in a VACTERL patient

(2008) Maria-Mercè Garcia-Barceló et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Germ cells and transgenesis in chickens

(2008) Jae Yong Han   COMPARATIVE IMMUNOLOGY MICROBIOLOGY AND INFECTIOUS DISEASES