Studies ofTBX4and chromosome 17q23.1q23.2: An uncommon cause of nonsyndromic clubfoot

Variants in genes that encode muscle contractile proteins influence risk for isolated clubfoot

(2011) Katelyn S. Weymouth et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

cis-regulatory mutations are a genetic cause of human limb malformations

(2011) Julia E. VanderMeer et al.   DEVELOPMENTAL DYNAMICS

Familial Isolated Clubfoot Is Associated with Recurrent Chromosome 17q23.1q23.2 Microduplications Containing TBX4

(2010) David M. Alvarado et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Identification of a Recurrent Microdeletion at 17q23.1q23.2 Flanked by Segmental Duplications Associated with Heart Defects and Limb Abnormalities

(2010) Blake C. Ballif et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Tbx4 and Tbx5 Acting in Connective Tissue Are Required for Limb Muscle and Tendon Patterning

(2010) Peleg Hasson et al.   DEVELOPMENTAL CELL

Detection of clinically relevant exonic copy-number changes by array CGH

(2010) Philip M. Boone et al.   HUMAN MUTATION

Altered transmission ofHOXand apoptotic SNPs identify a potential common pathway for clubfoot

(2009) Audrey R. Ester et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Impact of congenital talipes equinovarus etiology on treatment outcomes

(2009) Christina A Gurnett et al.   DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY

Dual hindlimb control elements in the Tbx4 gene and region-specific control of bone size in vertebrate limbs

(2008) D. B. Menke et al.   DEVELOPMENT