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Oxford University Press

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Paternal origin of FGFR3 mutations in Muenke-type craniosynostosis

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Human Genetics, Vol. 115, Iss. 3, 2004-08 ,pp. : 200-207

Springer Publishing Company

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Abnormal FGFR 3 Expression in Cartilage of Thanatophoric Dysplasia Fetuses

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Defective bone mineralization and osteopenia in young adult FGFR3 −/− mice

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FGFR3 is a target of the homeobox transcription factor SHOX in limb development

By Decker Eva   Durand Claudia   Bender Sebastian   Rödelsperger Christian   Glaser Anne   Hecht Jochen   Schneider Katja U.   Rappold Gudrun  

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