FGFR3 promotes synchondrosis closure and fusion of ossification centers through the MAPK pathway von Matsushita, Takehiko, Wilcox, William R., Chan, Yuk Yu, Kawanami, Aya, Bükülmez, Hülya, Balmes, Gener, Krejci, Pavel, Mekikian, Pertchoui B., Otani, Kazuyuki, Yamaura, Isakichi, Warman, Matthew L., Givol, David, Murakami, Shunichi

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The fibroblast growth factors in multiple myeloma von Krejci, P, Mekikian, P B, Wilcox, W R

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Interaction of fibroblast growth factor and C-natriuretic peptide signaling in regulation of chondrocyte proliferation and extracellular matrix homeostasis von Krejci, Pavel, Masri, Bernard, Fontaine, Vincent, Mekikian, Pertchoui B, Weis, MaryAnn, Prats, Herve, Wilcox, William R

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121 PROGRESSIVE DIAPHYSEAL DYSPLASIA (CAMURATI-ENGELMANN DISEASE): REPORT OF A FOUR-GENERATION PEDIGREE, REVIEW OF THE LITERATURE, AND IDENTIFICATION OF MUTATIONS IN TRANSFORMING G... von Wallace, S. E., Lachman, R. S., Mekikian, P. B., Bui, K. K., Wilcox, W. R.

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Extra pelvic ossification centers in thanatophoric dysplasia and platyspondylic lethal skeletal dysplasia-San Diego type von Kitoh, H, Lachman, R S, Brodie, S G, Mekikian, P B, Rimoin, D L, Wilcox, W R

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Marked phenotypic variability in progressive diaphyseal dysplasia (Camurati-Engelmann disease): Report of a four-generation pedigree, identification of a mutation in TGFB1, and rev... von Wallace, Stephanie E., Lachman, Ralph S., Mekikian, Pertchoui B., Bui, Kathy K., Wilcox, William R.

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Platyspondylic lethal skeletal dysplasia, San Diego type, is caused by FGFR3 mutations von Brodie, Steven G., Kitoh, Hiroshi, Lachman, Ralph S., Nolasco, Loyda M., Mekikian, Pertchoui B., Wilcox, William R.

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Lethal osteosclerotic skeletal dysplasia with intracellular inclusion bodies von Brodie, Steven G., Lachman, Ralph S., McGovern, Margaret M., Mekikian, Pertchoui B., Wilcox, William R.

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PROGRESSIVE DIAPHYSEAL DYSPLASIA (CAMURATI-ENGELMANN DISEASE): REPORT OF A FOUR-GENERATION PEDIGREE, REVIEW OF THE LITERATURE, AND IDENTIFICATION OF MUTATIONS IN TRANSFORMING GROWT... von Wallace, S. E., Lachman, R. S., Mekikian, P. B., Bui, K. K., Wilcox, W. R.

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Mutations in the EVC1 gene are not a common finding in the Ellis-van Creveld and short rib-polydactyly type III syndromes von Takamine, Yuji, Krejci, Pavel, Mekikian, Pertchoui B., Wilcox, William R.

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Lethal Osteosclerotic Skeletal Dysplasia With Intracellular Inclusion Bodies von Brodie, S G, Lachman, R S, McGovern, M M, Mekikian, P B, Wilcox, W R

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