Functional haploinsufficiency of the human homeobox gene MSX2 causes defects in skull ossification

A comprehensive genetic map of the human genome based on 5,264 microsatellites

Colette Dib, Sabine Fauré, Cécile Fizames et al. · Nature · 1996 · 3K citations

Life Sciences, Genetics, Molecular Genetics +12

Mutations Involving the Transcription Factor CBFA1 Cause Cleidocranial Dysplasia

Stefan Mundlos, F Otto, C Mundlos et al. · Cell · 1997 · 1.5K citations · Full text

Dentistry, Genetics, Molecular Genetics +7

Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation

Ichiro Satokata, Liang Ma, Hayato Ohshima et al. · Nature Genetics · 2000 · 740 citations

Medicine, Craniofacial Biology, Developmental Biology +13

A human MSX1 homeodomain missense mutation causes selective tooth agenesis

Heleni Vastardis, Nadeem Y. Karimbux, Symon W. Guthua et al. · Nature Genetics · 1996 · 723 citations

Dentistry, Oral Biology, Oral Pathology +9

A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis

Ethylin Wang Jabs, Ulrich Müller, Xiang Li et al. · Cell · 1993 · 680 citations

Medicine, Genetics, Molecular Genetics +14