Rowan Digital Works

Physical map and characterization of transcripts in the candidate interval for familial chondrocalcinosis at chromosome 5p15.1., K. Rojas, L. Serrano de la Peña, T. Gallardo, A. Simmons, K. Nyce, R. McGrath, E. Considine, A.J. Vasko, E. Peterson, D. Grady, R. Cox, L.J. Andrew, M. Lovett, J. Overhauser, C.J. Williams
Charlene Williams

A−2→G transition at the 3′ acceptor splice site of IVS17 characterizes the COL2A1 gene mutation in the original stickler syndrome kindred, C. J. Williams, A. Ganguly, E. Considine, S. McCarron, D. J. Prockop, C. Walsh-Vockley, V. V. Michels
Charlene Williams

A single base mutation in the type II procollagen gene (COL2A1) that converts glycine α1‐247 to serine in a family with late‐onset spondyloepiphyseal dysplasia, P. Ritvaniemi, B. P. Sokolov, C. J. Williams, E. Considine, L. Yurgenev, E. M. Meerson, L. Ala-Kokko, D. J. Prockop
Charlene Williams