Philippe Debeer

Loss-of-function mutations in LEMD3 result in osteopoikilosis, Buschke-Ollendorff syndrome and melorheostosis

Jan Hellemans, Olena Preobrazhenska, Andy Willaert et al. · Nature Genetics · 2004 · 454 citations · Full text

Lemd3 Result, Developmental Biology, Sclerostin +9

PA26 is a candidate gene for heterotaxia in humans: identification of a novel PA26-related gene family in human and mouse

Hilde Peeters, Philippe Debeer, Amos Bairoch et al. · Human Genetics · 2003 · 114 citations

Genetic Disorder, Genetics, Molecular Genetics +4

The fibulin-1 gene <i>(FBLN1)</i> is disrupted in a t(12;22) associated with a complex type of synpolydactyly

Philippe Debeer · Journal of Medical Genetics · 2002 · 103 citations · Full text

GermlineLEMD3 mutations are rare in sporadic patients with isolated melorheostosis

Jan Hellemans, Philippe Debeer, Michael Wright et al. · Human Mutation · 2006 · 81 citations

Sclerostin, Bone Morphogenic Protein, Genetic Disorder +14

Treatment of rotator cuff arthropathy with a reversed Delta shoulder prosthesis.

Reinhilde Jacobs, Philippe Debeer, Luc De Smet · PubMed · 2001 · 73 citations

Reversed Shoulder Prosthesis, Orthopaedics, Rotator Cuff +10