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American Journal of Medical Genetics|January 25, 1992
Study of color vision in fragile X syndromeB M Finucane, E Jaeger, E Dunn, et al.Matrix Biology : Journal of the International Society for Matrix Biology|February 27, 2001
Analysis of the promoter region of human cartilage oligomeric matrix protein (COMP)M Deere, C Rhoades Hall, K B Gunning, et al.American Journal of Human Genetics|May 1, 1995
Hereditary multiple exostosis and chondrosarcoma: linkage to chromosome II and loss of heterozygosity for EXT-linked markers on chromosomes II and 8J T Hecht, D Hogue, L C Strong, et al.Annals of Neurology|July 1, 1988
Neurological basis of respiratory complications in achondroplasiaF W Nelson, J T Hecht, W A Horton, et al.Neurology|November 18, 1998
Expanding the phenotype of the 8344 transfer RNAlysine mitochondrial DNA mutationS A Austin, F J Vriesendorp, F T Thandroyen, et al.American Journal of Medical Genetics|November 1, 1988
Obesity in achondroplasiaJ T Hecht, O J Hood, R J Schwartz, et al.American Journal of Medical Genetics|September 19, 1998
Segregation analysis of idiopathic talipes equinovarus in a Texan populationM de Andrade, J S Barnholtz, C I Amos, et al.Genome Research|May 18, 1999
Genomic characterization of human DSPG3M Deere, J L Dieguez, S J Yoon, et al.American Journal of Medical Genetics|March 1, 1992
Growth hormone therapy in achondroplasiaW A Horton, J T Hecht, O J Hood, et al.American Journal of Medical Genetics|February 15, 1993
Mosaicism for deletion 17p11.2 in a boy with the Smith-Magenis syndromeB M Finucane, M B Kurtz, V R Babu, et al.Pageof 14