Concepedia

A Nonsense Mutation in MSX1 Causes Witkop Syndrome

Dolrudee Jumlongras, Marianna Bei, Jean M. Stimson, Wen-Fang Wang, Steven R. DePalma, Christine E. Seidman, Ute Felbor, Richard L. Maas, Jonathan G. Seidman, Bjørn R. Olsen

The American Journal of Human Genetics · 2001 · 263 citations · 21 references

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21

Msx1 deficient mice exhibit cleft palate and abnormalities of craniofacial and tooth development

Ichiro Satokata, Richard L. Maas · Nature Genetics · 1994 · 1.3K citations

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X–linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane protein

Juha Kere, Anand Srivastava, Outi Montonen et al. · Nature Genetics · 1996 · 756 citations

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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

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MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans

Marie‐José H. van den Boogaard, M. Dorland, Frits A. Beemer et al. · Nature Genetics · 2000 · 587 citations

, , +16

Dual roles of Wnt signaling during chondrogenesis in the chicken limb

Christine Hartmann, Clifford J. Tabin · Development · 2000 · 471 citations

, , +17