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Results: 5

Authors: Vargas, J Cox, GF Korf, BR
Citation: J. Vargas et al., Response to letter to the editor by zenker - "Diagnosis of FS should not be made until PKS is ruled out", AM J MED G, 102(3), 2001, pp. 307-307

Authors: Vargas, JE Cox, GF Korf, BR
Citation: Je. Vargas et al., Discordant phenotype in monozygotic twins with Fryns syndrome, AM J MED G, 94(1), 2000, pp. 42-45

Authors: Bonnemann, CG Cox, GF Shapiro, F Wu, JJ Feener, CA Thompson, TG Anthony, DC Eyre, DR Darras, BT Kunkel, LM
Citation: Cg. Bonnemann et al., A mutation in the alpha 3 chain of type IX collagen causes autosomal dominant multiple epiphyseal dysplasia with mild myopathy, P NAS US, 97(3), 2000, pp. 1212-1217

Authors: Grenier, MA Osganian, SK Cox, GF Towbin, JA Colan, SD Lurie, PR Sleeper, LA Orav, EJ Lipshultz, SE
Citation: Ma. Grenier et al., Design and implementation of the North American Pediatric Cardiomyopathy Registry, AM HEART J, 139(2), 2000, pp. S86-S95

Authors: Annunen, S Korkko, J Czarny, M Warman, ML Brunner, HG Kaariainen, H Mulliken, JB Tranebjaerg, L Brooks, DG Cox, GF Cruysberg, JR Curtis, MA Davenport, SLH Friedrich, CA Kaitila, I Krawczynski, MR Latos-Bielenska, A Mukai, S Olsen, BR Shinno, N Somer, M Vikkula, M Zlotogora, J Prockop, DJ Ala-Kokko, L
Citation: S. Annunen et al., Splicing mutations of 54-bp exons in the COL11A1 gene cause Marshall syndrome, but other mutations cause overlapping Marshall/Stickler phenotypes, AM J HU GEN, 65(4), 1999, pp. 974-983
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