Concepedia

Satb2 Haploinsufficiency Phenocopies 2q32-q33 Deletions, whereas Loss Suggests a Fundamental Role in the Coordination of Jaw Development

Olga V. Britanova, Michael J. Depew, Manuela Schwark, Bethan Thomas, Isabelle Milétich, Paul T. Sharpe, Victor Tarabykin

The American Journal of Human Genetics · 2006 · 184 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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DiGeorge syndrome phenotype in mice mutant for the T-box gene, Tbx1

Loydie A. Jerome, Virginia E. Papaioannou · Nature Genetics · 2001 · 1.1K citations

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Role of TBX1 in human del22q11.2 syndrome

Hisato Yagi, Yoshiyuki Furutani, Hiromichi Hamada et al. · The Lancet · 2003 · 880 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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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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