Pages that link to "Q59093569"

The following pages link to Quantification of the close association between DNA haplotypes and specific β-thalassaemia mutations in Mediterraneans (Q59093569):

Displaying 50 items.

• Autosomal recessive chronic granulomatous disease caused by deletion at a dinucleotide repeat (Q24563767) (← links)
• 2013 William Allan Award: My multifactorial journey (Q28657851) (← links)
• Mutations linked to the pro alpha 2(I) collagen gene are responsible for several cases of osteogenesis imperfecta type I (Q33673710) (← links)
• Beta thalassaemia mutations in Sardinians: implications for prenatal diagnosis (Q33674273) (← links)
• Prenatal diagnosis of beta thalassaemia by oligonucleotide analysis in Mediterranean populations (Q33682063) (← links)
• Beta zero thalassemia caused by a base substitution that creates an alternative splice acceptor site in an intron (Q33880476) (← links)
• Genetic analysis of amplified DNA with immobilized sequence-specific oligonucleotide probes (Q34297073) (← links)
• Haplotypes and linkage disequilibrium at the phenylalanine hydroxylase locus, PAH, in a global representation of populations (Q34390644) (← links)
• Evaluation of "at risk" alpha 1-antitrypsin genotype SZ with synthetic oligonucleotide gene probes (Q34521234) (← links)
• The frequency and origin of the sickle cell mutation in the district of Coruche/Portugal (Q34531299) (← links)
• The phenylketonuria locus: current knowledge about alleles and mutations of the phenylalanine hydroxylase gene in various populations (Q34540558) (← links)
• Distribution of beta-thalassemia mutations in south China and their association with haplotypes (Q35199512) (← links)
• Evidence supporting a single origin of the beta(C)-globin gene in blacks (Q35200360) (← links)
• Extensive restriction site polymorphism at the human phenylalanine hydroxylase locus and application in prenatal diagnosis of phenylketonuria (Q35200406) (← links)
• Nonuniform recombination within the human beta-globin gene cluster (Q35200412) (← links)
• A strategy for using multiple linked markers for genetic counseling (Q35200505) (← links)
• Characterization of a spontaneous mutation to a beta-thalassemia allele (Q35200973) (← links)
• Identification of a beta-thalassemia mutation associated with a novel haplotype of RFLPs (Q35201018) (← links)
• Evidence for increased recombination near the human insulin gene: implication for disease association studies (Q35590864) (← links)
• Hematopoietic stem cells develop in the absence of endothelial cadherin 5 expression (Q36406985) (← links)
• Gene defects in beta-thalassemia and their prenatal diagnosis (Q36629953) (← links)
• Evolution of a genetic disease in an ethnic isolate: beta-thalassemia in the Jews of Kurdistan (Q37365779) (← links)
• On the origin and spread of beta-thalassemia: recurrent observation of four mutations in different ethnic groups (Q37397576) (← links)
• Chromosomal assignment of the human erythropoietin gene and its DNA polymorphism (Q37399458) (← links)
• Haplotypes linked to three rare beta-thalassemia mutations, originally reported in Tunisia (Q38908517) (← links)
• The peculiar spectrum of beta-thalassemia genes in Tunisia (Q38943999) (← links)
• Why are some genetic diseases common? Distinguishing selection from other processes by molecular analysis of globin gene variants (Q39006484) (← links)
• Beta-thalassemia in Algeria (Q39155512) (← links)
• Molecular characterization of beta-thalassemia mutations in Egypt (Q39310585) (← links)
• The evolution of the alpha- and beta-globin gene clusters in human populations (Q39743628) (← links)
• DNA polymorphism and molecular pathology of the human globin gene clusters (Q39813814) (← links)
• Beta-thalassemia genes in French-Canadians: haplotype and mutation analysis of Portneuf chromosomes. (Q40578936) (← links)
• Molecular diagnostics: past, present, and future (Q40789080) (← links)
• Gametic equilibrium between 24 polymorphic markers (Q41186571) (← links)
• Correlation between polymorphic DNA haplotypes at phenylalanine hydroxylase locus and clinical phenotypes of phenylketonuria (Q41342853) (← links)
• Heterogeneity of haplotypes among patients with severe Cooley disease in Eastern Sicily (Q41360171) (← links)
• Tracing the mutations in cystic fibrosis by means of closely linked DNA markers (Q41924406) (← links)
• Novel promoter and splice junction defects add to the genetic, clinical or geographic heterogeneity of ?-thalassaemia in the Portuguese population (Q43580920) (← links)
• Mediterranean types of beta-thalassemia in the German population (Q43982571) (← links)
• Mutation analysis of beta-thalassemia genes in a German family reveals a rare transversion in the first intron (Q44168157) (← links)
• The spectrum of β-thalassaemia mutations in Sicily (Q44624896) (← links)
• Intrinsic potential for high fetal hemoglobin production in a Druz family with beta-thalassemia is due to an unlinked genetic determinant (Q45365529) (← links)
• Unexpected pattern of beta-globin mutations in beta-thalassaemia patients from northern Portugal (Q46321318) (← links)
• Fifty years in human genetics--a career retrospective (Q50240771) (← links)
• Molecular basis of thalassemia syndromes in Serbia and Montenegro. (Q51479951) (← links)
• DNA polymorphism patterns in the beta-globin gene cluster in the Japanese population. (Q52258896) (← links)
• Thalassemia Syndromes in Serbia: An update (Q54410411) (← links)
• β-Thalassemia in China: a Systematic Molecular Characterization of β-Thalassemia Mutations (Q57162514) (← links)
• A candidate for the cystic fibrosis locus isolated by selection for methylation-free islands (Q57304822) (← links)
• A comparison of sickle cell syndromes in Northern Greece (Q57397805) (← links)