Nucleation of monosodium urate crystals.

Por Wilcox, W R, Khalaf, A A
Publicado em 1975

Factors affecting urate solubility in vitro.

Por Kippen, I, Klinenberg, J R, Weinberger, A, Wilcox, W R
Publicado em 1974

High molecular weight FGF2: the biology of a nuclear growth factor

Por Chlebova, K., Bryja, V., Dvorak, P., Kozubik, A., Wilcox, W. R., Krejci, P.
Publicado em 2009

Atelosteogenesis type II is caused by mutations in the diastrophic dysplasia sulfate-transporter gene (DTDST): evidence for a phenotypic series involving three chondrodysplasias.

Por Hästbacka, J., Superti-Furga, A., Wilcox, W. R., Rimoin, D. L., Cohn, D. H., Lander, E. S.
Publicado em 1996

Expression, in cartilage, of a 7-amino-acid deletion in type II collagen from two unrelated individuals with Kniest dysplasia.

Por Bogaert, R., Wilkin, D., Wilcox, W. R., Lachman, R., Rimoin, D., Cohn, D. H., Eyre, D. R.
Publicado em 1994

Spondylo-mesomelic-acrodysplasia with joint dislocations and severe combined immunodeficiency: a newly recognised immuno-osseous dysplasia.

Por Castriota-Scanderbeg, A, Mingarelli, R, Caramia, G, Osimani, P, Lachman, R S, Rimoin, D L, Wilcox, W R, Dallapiccola, B
Publicado em 1997

Diverse mutations in the gene for cartilage oligomeric matrix protein in the pseudoachondroplasia-multiple epiphyseal dysplasia disease spectrum.

Por Briggs, M D, Mortier, G R, Cole, W G, King, L M, Golik, S S, Bonaventure, J, Nuytinck, L, De Paepe, A, Leroy, J G, Biesecker, L, Lipson, M, Wilcox, W R, Lachman, R S, Rimoin, D L, Knowlton, R G, Cohn, D H
Publicado em 1998

A novel skeletal dysplasia with developmental delay and acanthosis nigricans is caused by a Lys650Met mutation in the fibroblast growth factor receptor 3 gene.

Por Tavormina, P L, Bellus, G A, Webster, M K, Bamshad, M J, Fraley, A E, McIntosh, I, Szabo, J, Jiang, W, Jabs, E W, Wilcox, W R, Wasmuth, J J, Donoghue, D J, Thompson, L M, Francomano, C A
Publicado em 1999