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Nature Genetics|December 30, 1999
Mutations in a new photoreceptor-pineal gene on 17p cause Leber congenital amaurosisM M Sohocki, S J Bowne, L S Sullivan, et al.Journal of Human Hypertension|June 3, 2016
Utility of blood pressure genetic risk score in admixed Hispanic samplesA H Beecham, L Wang, N Vasudeva, et al.The Journal of Heart and Lung Transplantation : the Official Publication of the International Society for Heart Transplantation|September 1, 1991
Acute vascular rejection of the coronary arteries in human heart transplantation: pathology and correlations with immunosuppression and cytomegalovirus infectionS J Normann, D R Salomon, P Leelachaikul, et al.Human Heredity|May 9, 2000
Fine mapping of the human biotinidase gene and haplotype analysis of five common mutationsS H Blanton, A Pandya, B L Landa, et al.Journal of Medical Genetics|August 6, 2002
A novel locus for autosomal dominant non-syndromic deafness (DFNA41) maps to chromosome 12q24-qterS H Blanton, C Y Liang, M W Cai, et al.Scientific Reports|August 27, 2016
Variations in Multiple Syndromic Deafness Genes Mimic Non-syndromic Hearing LossG Bademci, F B Cengiz, J Foster Ii, et al.Journal of Dental Research|February 29, 2012
Association of AXIN2 with non-syndromic oral clefts in multiple populationsA Letra, B Bjork, M E Cooper, et al.Pageof 12