The Liebenberg syndrome: in depth analysis of the original family

Structural variations, the regulatory landscape of the genome and their alteration in human disease

(2013) Malte Spielmann et al.   BIOESSAYS

CNVs of noncoding cis-regulatory elements in human disease

(2013) Malte Spielmann et al.   CURRENT OPINION IN GENETICS & DEVELOPMENT

Liebenberg Syndrome: Case Report and Insight Into Molecular Basis

(2013) Hisham Abdel-Ghani et al.   JOURNAL OF HAND SURGERY-AMERICAN VOLUME

Homeotic Arm-to-Leg Transformation Associated with Genomic Rearrangements at the PITX1 Locus

(2012) Malte Spielmann et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Regulation of limb bud initiation and limb-type morphology

(2011) Veronique Duboc et al.   DEVELOPMENTAL DYNAMICS

Enhancer-adoption as a mechanism of human developmental disease

(2011) Laura A. Lettice et al.   HUMAN MUTATION

Histone variant macroH2A1 deletion in mice causes female-specific steatosis

(2010) Mathieu Boulard et al.   Epigenetics & Chromatin

Liebenberg Syndrome: First Case of Monovular Twins

(2009) Gianluigi Di Gennaro et al.   PLASTIC AND RECONSTRUCTIVE SURGERY

Adaptive Evolution of Pelvic Reduction in Sticklebacks by Recurrent Deletion of a Pitx1 Enhancer

(2009) Y. F. Chan et al.   SCIENCE