Concepedia

Clinical and functional data implicate the Arg(151)Ser variant of MSX1 in familial hypodontia

Munefumi Kamamoto, Junichiro Machida, Seishi Yamaguchi, Masashi Kimura, Takao Ono, Peter A. Jezewski, Yujiro Higashi, Atsuo Nakayama, Kazuo Shimozato, Yoshihito Tokita

European Journal of Human Genetics · 2011 · 29 citations · 52 references

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52

Personal genomes: The case of the missing heritability

Brendan A. Maher · Nature · 2008 · 1.8K citations · Full text

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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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<i>Pax9</i>-deficient mice lack pharyngeal pouch derivatives and teeth and exhibit craniofacial and limb abnormalities

Heiko Peters, Annette Neubüser, Klaus Kratochwil et al. · Genes & Development · 1998 · 832 citations · Full text

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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

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