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Current Genetics|April 1, 1992
The nucleotide sequence of the small subunit ribosomal RNA gene from Symbiodinium pilosum, a symbiotic dinoflagellateL A Sadler, K L McNally, N S Govind, et al.Cytogenetics and Cell Genetics|January 1, 1989
Exclusion of Usher syndrome gene from much of chromosome 4R J Smith, J D Holcomb, S P Daiger, et al.American Journal of Human Genetics|October 30, 1998
A range of clinical phenotypes associated with mutations in CRX, a photoreceptor transcription-factor geneM M Sohocki, L S Sullivan, H A Mintz-Hittner, et al.American Journal of Human Genetics|April 1, 1989
Autosomal dominant retinitis pigmentosa: exclusion of the gene from the short arm of chromosome 1 including the region surrounding the rhesus locusD G Bradley, G J Farrar, E M Sharp, et al.Genomics|June 14, 2000
Confirmation of the mapping of the Camurati-Englemann locus to 19q13. 2 and refinement to a 3.2-cM regionS P Vaughn, S Broussard, C R Hall, et al.Genomics|December 1, 1992
Localization of two genes for Usher syndrome type I to chromosome 11R J Smith, E C Lee, W J Kimberling, et al.American Journal of Medical Genetics|July 13, 2002
Testing for genetic associations with the PAX gene family in a spina bifida populationK A Volcik, S H Blanton, M C Kruzel, et al.American Journal of Medical Genetics|July 13, 2002
Testing for genetic associations in a spina bifida population: analysis of the HOX gene family and human candidate gene regions implicated by mouse models of neural tube defectsK A Volcik, S H Blanton, M C Kruzel, et al.Human Genetics|June 21, 2001
Connexin 26 (GJB2) mutations in the Turkish population: implications for the origin and high frequency of the 35delG mutation in CaucasiansM Tekin, N Akar, S Cin, et al.American Journal of Medical Genetics|June 1, 1994
Refined localization of the branchiootorenal syndrome gene by linkage and haplotype analysisL Ni, M J Wagner, W J Kimberling, et al.Pageof 12