Prenatal diagnosis of a 7p15-p21 deletion encompassing the TWIST1 gene involved in Saethre–Chotzen syndrome

Mutations of the TWIST gene in the Saethre-Chotzene syndrome

Vincent El Ghouzzi, M Le Merrer, Fabienne Perrin‐Schmitt et al. · Nature Genetics · 1997 · 644 citations

Life Sciences, Genetics, Molecular Genetics +7

A Comprehensive Screen for TWIST Mutations in Patients with Craniosynostosis Identifies a New Microdeletion Syndrome of Chromosome Band 7p21.1

David Johnson, Sharon W. Horsley, Dominique M. Moloney et al. · The American Journal of Human Genetics · 1998 · 230 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

An HF-1a/ HF-1b/MEF-2 combinatorial element confers cardiac ventricular specificity and establishes an anterior-posterior gradient of expression

Robert S. Ross, Sutip Navankasattusas, Richard P. Harvey et al. · Development · 1996 · 125 citations

Life Sciences, Genetics, Molecular Genetics +17

<i>Hoxa11</i>and<i>Hoxd11</i>regulate branching morphogenesis of the ureteric bud in the developing kidney

Larry T. Patterson, Martina Pembaur, S. Steven Potter · Development · 2001 · 122 citations

Life Sciences, Developmental Biology, Genetics +17

Prenatal ultrasound diagnosis of fetal craniosynostosis

Sophie Delahaye, J Bernard, Dominique Rénier et al. · Ultrasound in Obstetrics and Gynecology · 2003 · 122 citations · Full text

Medicine, Pediatrics, Craniofacial Development +9