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GLI3 is rarely implicated in OFD syndromes with midline abnormalities.
Avila, M; Gigot, N; Aral, B; Callier, P; Gautier, E; Thevenon, J; Pasquier, L; Lopez, E; Gueneau, L; Duplomb, L; Goldenberg, A; Baumann, C; Cormier, V; Marlin, S; Masurel-Paulet, A; Huet, F; Attié-Bitach, T; Faivre, L; Thauvin-Robinet, C.
Hum Mutat ; 32(11): 1332-3, 2011 Nov.
Article in En | MEDLINE | ID: mdl-21796731
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Abnormalities, Multiple / Polydactyly / Syndactyly / Kruppel-Like Transcription Factors / Pallister-Hall Syndrome / Mutation / Nerve Tissue Proteins Limits: Humans Language: En Journal: Hum Mutat Year: 2011 Document type: Article
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Abnormalities, Multiple / Polydactyly / Syndactyly / Kruppel-Like Transcription Factors / Pallister-Hall Syndrome / Mutation / Nerve Tissue Proteins Limits: Humans Language: En Journal: Hum Mutat Year: 2011 Document type: Article