DNA haplotypes in the G6PD gene cluster studied in the Chinese Li population and their relationship to G6PDCanton.

No abstract is available for this paper.

• Publication year

  1994

• Venue

  Human Heredity

• Publication date

  1994-09-01

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1159/000154230PMID 7927357
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Genetic heterogeneity of glucose-6-phosphate dehydrogenase deficiency revealed by single-strand conformation and sequence analysis.

  1993cited by this paper
• Molecular characterization of glucose-6-phosphate dehydrogenase (G6PD) deficiency in patients of Chinese descent and identification of new base substitutions in the human G6PD gene.

  1993cited by this paper
• G6PD haplotypes spanning Xq28 from F8C to red/green color vision.

  1993cited by this paper
• Haplotype diversity in the human red and green opsin genes: evidence for frequent sequence exchange in exon 3.

  1993cited by this paper
• A new polymorphic site in the G6PD gene

  1992cited by this paper
• Identification of novel RFLPs in the vicinity of CpG islands in Xq28: application to the analysis of the pattern of X chromosome inactivation.

  1992cited by this paper
• A new mutation responsible for severe G6PD deficiency in two ethnic Chinese with different clinical presentations: determination by a direct PCR sequencing technique.

  1992cited by this paper
• Genome analysis and the human X chromosome.

  1992cited by this paper
• The molecular basis of glucose-6-phosphate dehydrogenase deficiency.

  1992cited by this paper
• Polymorphism in red photopigment underlies variation in colour matching

  1992cited by this paper
• Molecular characterization of glucose-6-phosphate dehydrogenase (G6PD) deficiency by natural and amplification created restriction sites: five mutations account for most G6PD deficiency cases in Taiwan.

  1992cited by this paper
• A to G substitution identified in exon 2 of the G6PD gene among G6PD deficient Chinese.

  1991cited by this paper
• Two commonly occurring nucleotide base substitutions in Chinese G6PD variants.

  1991cited by this paper
• The genetics of glucose-6-phosphate dehydrogenase deficiency.

  1990cited by this paper
• A PvuII restriction fragment length polymorphism of the glucose-6-phosphate dehydrogenase gene is an African-specific marker

  1990cited by this paper
• Origin and spread of the glucose-6-phosphate dehydrogenase variant (G6PD-Mediterranean) in the Middle East.

  1990cited by this paper
• G6PD Canton a common deficient variant in South East Asia caused by a 459 Arg----Leu mutation.

  1990cited by this paper
• The NT 1311 polymorphism of G6PD: G6PD Mediterranean mutation may have originated independently in Europe and Asia.

  1990cited by this paper
• RFLP of the X chromosome-linked glucose-6-phosphate dehydrogenase locus in blacks.

  1988cited by this paper
• Globin genes are useful markers to identify genetic similarities between Fijians and Pacific Islanders from Polynesia and Melanesia.

  1988cited by this paper
• An extensive search for RFLP in the human glucose-6-phosphate dehydrogenase locus has revealed a silent mutation in the coding sequence.

  1988cited by this paper
• A new Hind III restriction fragment length polymorphism in the hemophilia A locus

  1987cited by this paper
• A new polymorphism in the factor VIII gene for prenatal diagnosis of hemophilia A.

  1986cited by this paper
• The evolution of the alpha- and beta-globin gene clusters in human populations.

  1986cited by this paper
• Evolutionary relationships of human populations from an analysis of nuclear DNA polymorphisms

  1986cited by this paper
• Linkage disequilibrium for two X-linked genes in Sardinia and its bearing on the statistical mapping of the human X chromosome.

  1977cited by this paper
• Estimation of linkage disequilibrium in randomly mating populations

  1974cited by this paper
• Glucose‐6‐phosphate dehydrogenase, colour vision and Xg blood groups in Greece: linkage and population data

  1963cited by this paper

• Chinese newborn screening for the incidence of G6PD deficiency and variant of G6PD gene from 2013 to 2017

  2019cites this paper
• Human Mutation

  2019cites this paper
• Significance of 3′UTR and Pathogenic Haplotype in Glucose-6-Phosphate Deficiency

  2017cites this paper
• Estimation of G6pd Status in the Rajbangshi Population of Sushrutanagar

  2013cites this paper
• The spatial epidemiology of the Duffy blood group and G6PD deficiency

  2012cites this paper
• Differential structuring of human populations for homologous X and Y microsatellite loci.

  1997cites this paper
• Rapid detection of common Chinese glucose-6-phosphate dehydrogenase (G6PD) mutations by denaturing gradient gel electrophoresis (DGGE).

  1996cites this paper
• Novel tetranucleotide repeat polymorphism in the human adenosine deaminase gene: interethnic comparison of three major human groups.

  1996cites this paper
• two families with novel mutations causing G6PD

  year unknowncites this paper