Erratum: Identification of the Cystic Fibrosis Gene: Genetic Analysis
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L. Tsui | J. Rommens | B. Kerem | A. Chakravarti | J. Buchanan | M. Buchwald | D. Markiewicz | T. Cox
[1] L. Tsui,et al. Erratum: Identification of the Cystic Fibrosis Gene: Cloning and Characterization of Complementary DNA , 1989, Science.
[2] J. Riordan,et al. Identification of the Cystic Fibrosis Gene : Chromosome Walking and Jumping Author ( s ) : , 2008 .
[3] S. Daiger,et al. Polymorphic DNA haplotypes at the phenylalanine hydroxylase (PAH) locus in European families with phenylketonuria (PKU). , 1989, American journal of human genetics.
[4] M. Corey,et al. Familial concordance of pancreatic function in cystic fibrosis. , 1989, The Journal of pediatrics.
[5] M. Corey,et al. DNA marker haplotype association with pancreatic sufficiency in cystic fibrosis. , 1989, American journal of human genetics.
[6] M. Corey,et al. Clinical and genetic comparisons of patients with cystic fibrosis, with or without meconium ileus. , 1989, The Journal of pediatrics.
[7] X. Estivill,et al. Isolation of a new DNA marker in linkage disequilibrium with cystic fibrosis, situated between J3.11 (D7S8) and IRP. , 1989, American journal of human genetics.
[8] F. Collins,et al. Isolation of additional polymorphic clones from the cystic fibrosis region, using chromosome jumping from D7S8. , 1989, American journal of human genetics.
[9] K. Klinger,et al. Genealogical analysis of cystic fibrosis families and chromosome 7q RFLP haplotypes in the Hutterite Brethren. , 1989, American journal of human genetics.
[10] A. Beaudet,et al. Linkage disequilibrium, cystic fibrosis, and genetic counseling. , 1989, American journal of human genetics.
[11] L. Tsui. Tracing the mutations in cystic fibrosis by means of closely linked DNA markers. , 1989, American journal of human genetics.
[12] P. Green,et al. A 12 megabase restriction map at the cystic fibrosis locus. , 1989, Nucleic acids research.
[13] Charles R.scriver,et al. The Metabolic basis of inherited disease , 1989 .
[14] K. Buetow,et al. Analysis of DNA polymorphism haplotypes linked to the cystic fibrosis locus in North American black and Caucasian families supports the existence of multiple mutations of the cystic fibrosis gene. , 1989, American journal of human genetics.
[15] S. Woo. Collation of RFLP haplotypes at the human phenylalanine hydroxylase (PAH) locus. , 1988, American journal of human genetics.
[16] J. Rommens,et al. Identification and regional localization of DNA markers on chromosome 7 for the cloning of the cystic fibrosis gene. , 1988, American journal of human genetics.
[17] A. Beaudet,et al. Recombinations between IRP and cystic fibrosis. , 1988, American journal of human genetics.
[18] M. Dean,et al. Molecular and genetic analysis of cystic fibrosis. , 1988, Genomics.
[19] X. Estivill,et al. Linkage disequilibrium between cystic fibrosis and linked DNA polymorphisms in Italian families: a collaborative study. , 1988, American journal of human genetics.
[20] G. Lathrop,et al. A test of the heterozygote-advantage hypothesis in cystic fibrosis carriers. , 1988, American journal of human genetics.
[21] A. Poustka,et al. A long-range restriction map encompassing the cystic fibrosis locus and its closely linked genetic markers. , 1988, Genomics.
[22] F. Collins,et al. Physical mapping of the cystic fibrosis region by pulsed-field gel electrophoresis. , 1988, Genomics.
[23] P. Green,et al. Prenatal Diagnosis of Cystic Fibrosis by Chorionic Villus Sampling Using 12 Polymorphic Deoxyribonucleic Acid Markers , 1988, Obstetrics and gynecology.
[24] K. Mullis,et al. Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase. , 1988, Science.
[25] X. Estivill,et al. Experience with new DNA markers for the diagnosis of cystic fibrosis. , 1988, The New England journal of medicine.
[26] Y. Nakamura,et al. Refined linkage map of chromosome 7 in the region of the cystic fibrosis gene. , 1988, American journal of human genetics.
[27] C. Ober,et al. Studies of cystic fibrosis in Hutterite families by using linked DNA probes. , 1987, American journal of human genetics.
[28] X. Estivill,et al. Patterns of polymorphism and linkage disequilibrium for cystic fibrosis. , 1987, Genomics.
[29] A. Read,et al. CLINIC EXPERIENCE OF PRENATAL DIAGNOSIS OF CYSTIC FIBROSIS BY USE OF LINKED DNA PROBES , 1987, The Lancet.
[30] R. Meindl. Hypothesis: a selective advantage for cystic fibrosis heterozygotes. , 1987, American journal of physical anthropology.
[31] X. Estivill,et al. A candidate for the cystic fibrosis locus isolated by selection for methylation-free islands , 1987, Nature.
[32] D. Pritchard. Why cystic fibrosis is on the increase , 1987, Nature.
[33] L. Tsui,et al. Genetic analysis of cystic fibrosis using linked DNA markers. , 1986, American journal of human genetics.
[34] Y. Nakamura,et al. Further linkage data on cystic fibrosis: the Utah Study. , 1986, American journal of human genetics.
[35] A. Beaudet,et al. Linkage of DNA markers to cystic fibrosis in 26 families. , 1986, American journal of human genetics.
[36] Genetic homogeneity of cystic fibrosis. , 1986, Nucleic acids research.
[37] M. Farrall,et al. FIRST-TRIMESTER PRENATAL DIAGNOSIS OF CYSTIC FIBROSIS WITH LINKED DNA PROBES , 1986, The Lancet.
[38] K. Lange. Approximate confidence intervals for risk prediction in genetic counseling. , 1986, American journal of human genetics.
[39] L. Tsui,et al. Linkage between the loci for cystic fibrosis and paraoxonase , 1986, Clinical genetics.
[40] L. Tsui,et al. Mapping of the cystic fibrosis locus on chromosome 7. , 1986, Cold Spring Harbor symposia on quantitative biology.
[41] K. Mullis,et al. Enzymatic amplification of beta-globin genomic sequences and restriction site analysis for diagnosis of sickle cell anemia. , 1985, Science.
[42] L. Tsui,et al. Cystic Fibrosis Locus Defined by a Genetically Linked Polymorphic Dna Marker Author(s): Lap , 2022 .
[43] D. Cox,et al. DNA restriction fragments associated with α1-antitrypsin indicate a single origin for deficiency allele PI Z , 1985, Nature.
[44] Peter J. Scambler,et al. Localization of cystic fibrosis locus to human chromosome 7cen–q22 , 1985, Nature.
[45] Michael Dean,et al. A closely linked genetic marker for cystic fibrosis , 1985, Nature.
[46] L. Tsui,et al. A polymorphic DNA marker linked to cystic fibrosis is located on chromosome 7 , 1985, Nature.
[47] K. Buetow,et al. Nonuniform recombination within the human beta-globin gene cluster. , 1984, American journal of human genetics.
[48] S. Orkin,et al. Quantification of the close association between DNA haplotypes and specific β-thalassaemia mutations in Mediterraneans , 1984, Nature.
[49] A. Motulsky,et al. Linkage disequilibrium and evolutionary relationships of DNA variants (restriction enzyme fragment length polymorphisms) at the serum albumin locus. , 1984, Proceedings of the National Academy of Sciences of the United States of America.
[50] S. Antonarakis,et al. Origin of the beta S-globin gene in blacks: the contribution of recurrent mutation or gene conversion or both. , 1984, Proceedings of the National Academy of Sciences of the United States of America.
[51] P. Durie,et al. Colipase and lipase secretion in childhood-onset pancreatic insufficiency: Delineation of patients with steatorrhea secondary to relative colipase deficiency , 1984 .
[52] S. Antonarakis,et al. Hemoglobin E in Europeans: further evidence for multiple origins of the beta E-globin gene. , 1984, American journal of human genetics.
[53] S. Orkin,et al. The mutation and polymorphism of the human beta-globin gene and its surrounding DNA. , 1984, Annual review of genetics.
[54] R. Nelson,et al. Sex ratio and heterozygote advantage in cystic fibrosis families. , 1983, Archives of disease in childhood.
[55] H. Ostrer,et al. Evidence for multiple origins of the beta E-globin gene in Southeast Asia. , 1982, Proceedings of the National Academy of Sciences of the United States of America.
[56] M. Corey,et al. Improved respiratory prognosis in patients with cystic fibrosis with normal fat absorption. , 1982, The Journal of pediatrics.
[57] S. Antonarakis,et al. Nonrandom association of polymorphic restriction sites in the beta-globin gene cluster. , 1982, Proceedings of the National Academy of Sciences of the United States of America.
[58] Y. Kan,et al. Evolution of the hemoglobin S and C genes in world populations. , 1980, Science.
[59] Y. Kan,et al. Polymorphism of DNA Sequence in the β-Globin Gene Region , 1980 .
[60] Y. Kan,et al. Polymorphism of DNA sequence adjacent to human beta-globin structural gene: relationship to sickle mutation. , 1978, Proceedings of the National Academy of Sciences of the United States of America.
[61] J. Bodmer,et al. Evolution and function of the HLA system. , 1978, British medical bulletin.
[62] A. Burdick. Frequency of the gene for cystic fibrosis with a view of replacement and recognition effects and reproduction by homozygotes. , 1977, Human heredity.
[63] N. Morton,et al. Genetic studies on cystic fibrosis in Hawaii. , 1968, American journal of human genetics.
[64] A. Knudson,et al. On the selective advantage of cystic fibrosis heterozygotes. , 1967, American journal of human genetics.
[65] C. Anderson,et al. A genetic study of fibrocystic disease of the pancreas , 1965 .