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Complex Genetics of Glaucoma Susceptibility Richard T Libby
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Annual Review of Genomics and Human Genetics, Volume 8; Volume 2007
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abnormalities Acad activity affected allele amino acid analysis approach array CGH autoimmune diseases autosomal binding Biol biological cancer candidate genes cardiac cause cells CFTR cheetahs Chem chemical genetics chromosome Clin clinical clones comparative genomic complex compounds conserved copy number cystic fibrosis data sets deficiency deletion detection disease genes disorders domain encoding evolution factors Figure Genome Res genome sequence genotype glaucoma haplotype human disease human genome hypertrophic cardiomyopathy identified inactivation individuals interactions involved kinase linkage loci locus mammalian mapping meconium ileus mice microarray mitochondrial DNA molecular mouse mtDNA mutations myocyte myosin Natl Noonan syndrome nucleotide Ophthalmol pathways patients Pediatr phenotype phylogenetic polymorphisms population Proc protein psoriasis PTPN11 mutations receptor recombination region regulation role sarcomere Science screening SNPs specific structure suggest sulfatase SUMF1 susceptibility target taste tion tissue transcription troponin tumor variation VCAM1 ventricular X chromosome Xist