De novo inv(2)(p12q34) associated with Klippel-Feil anomaly and hypodontia

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

Online Mendelian Inheritance in Man

John Oyston · Anesthesiology · 1998 · 721 citations · Full text

Life Sciences, Biology, Genetics +4

Mutation of PAX9 is associated with oligodontia

David W. Stockton, Parimal Das, Monica Goldenberg et al. · Nature Genetics · 2000 · 528 citations

Life Sciences, Genetics, Molecular Genetics +6

Klippel-Feil Syndrome

Robert N. Hensinger, JOHN E. LANG, G. Dean MacEwen · Journal of Bone and Joint Surgery · 1974 · 372 citations

Medicine, Neurology, Cranial Nerve Disorders +10

Identification of a nonsense mutation in the PAX9 gene in molar oligodontia

Pekka Nieminen, Sirpa Arte, Dennis D. Tanner et al. · European Journal of Human Genetics · 2001 · 182 citations · Full text

Life Sciences, Genetics, Molecular Genetics +11