Craniosynostosis associated with ocular and distal limb defects is very likely caused by mutations in a gene different fromFGFR,TWIST, andMSX2-Reference-Cited by-同舟云学术

Craniosynostosis associated with ocular and distal limb defects is very likely caused by mutations in a gene different fromFGFR,TWIST, andMSX2

Published:2002-08-15 Issue:2 Volume:113 Page:200-206
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Passos-Bueno Maria Rita,Armelin Lucia Maria,Alonso Luís Garcia,Neustein Isaac,Sertié Andréa L.,Abe Kikue,Pavanello Rita de Cássia,Elkis Lívia C.,Koiffmann Célia P.

Funder

Fundação de Amparo a Pesquisa do Estado de São Paulo

Conselho Nacional de Pesquisa e Desenvolvimento

Programa dos Núcleos de Excelência

Howard Hughes Medical Institute

Publisher

Wiley

Subject

Genetics (clinical)

Reference24 articles.

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2. Identical mutations in three different fibroblast growth factor receptor genes in autosomal dominant craniosynostosis syndromes;Bellus;Nat Genet,1996

3. Fibroblast growth factor receptors: lessons from the genes;Burke;Trends Biochem Sci,1998

4. Mutations in TWIST genes in the Saethre-Choetzen syndrome;El Ghouzzi;Nat Genet,1997

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