Genome screening by searching for shared segments: mapping a gene for benign recurrent intrahepatic cholestasis
暂无分享,去创建一个
Nelson B. Freimer | N. Freimer | R. Houwen | L. Sandkuijl | J. Juyn | S. Baharloo | K. Blankenship | P. Raeymaekers | Lodewijk A. Sandkuijl | Roderick H. J. Houwen | Siamak Baharloo | Kathleen Blankenship | Peter Raeymaekers | Jenneke Juyn | Kathleen Blankenship
[1] V. Sheffield,et al. High resolution genetic maps incorporating multiple classes of short tandem repeat polymorphisms , 1994 .
[2] L. Sandkuijl,et al. Assignment of a gene for autosomal recessive retinitis pigmentosa (RP12) to chromosome 1q31-q32.1 in an inbred and genetically heterogeneous disease population. , 1994, Genomics.
[3] J. Weissenbach,et al. Close linkage to chromosome 3p and conservation of ancestral founding haplotype in hereditary nonpolyposis colorectal cancer families. , 1994, Proceedings of the National Academy of Sciences of the United States of America.
[4] M. Owen,et al. The genetic basis of complex human behaviors. , 1994, Science.
[5] Cécile Fizames,et al. The 1993–94 Généthon human genetic linkage map , 1994, Nature Genetics.
[6] N. Freimer,et al. Mutational processes of simple-sequence repeat loci in human populations. , 1994, Proceedings of the National Academy of Sciences of the United States of America.
[7] W. Bodmer,et al. Genetic steps in colorectal cancer , 1994, Nature Genetics.
[8] J. Seidman,et al. Homozygosity mapping of the gene for alkaptonuria to chromosome 3q2 , 1993, Nature genetics.
[9] J. Levy,et al. Availability of Type II Diabetic Families for Detection of Diabetes Susceptibility Genes , 1993, Diabetes.
[10] G. Gyapay,et al. Localization of Friedreich ataxia phenotype with selective vitamin E deficiency to chromosome 8q by homozygosity mapping , 1993, Nature genetics.
[11] E. Lander,et al. Localization of the EPM1 gene for progressive myoclonus epilepsy on chromosome 21: linkage disequilibrium allows high resolution mapping. , 1993, Human molecular genetics.
[12] Eric Lander,et al. Linkage disequilibrium mapping in isolated founder populations: diastrophic dysplasia in Finland , 1992, Nature Genetics.
[13] G. Gyapay,et al. A second-generation linkage map of the human genome , 1992, Nature.
[14] Hans Lehrach,et al. The Huntington's disease candidate region exhibits many different haplotypes , 1992, Nature Genetics.
[15] J. Weber,et al. A gene subject to genomic imprinting and responsible for hereditary paragangliomas maps to chromosome 11q23-qter. , 1992, Human molecular genetics.
[16] A. Geubel,et al. Benign recurrent intrahepatic cholestasis. A report of 26 cases. , 1989, Journal of clinical gastroenterology.
[17] L. Tsui,et al. Erratum: Identification of the Cystic Fibrosis Gene: Genetic Analysis , 1989, Science.
[18] R. Lewontin,et al. On measures of gametic disequilibrium. , 1988, Genetics.
[19] K. Lange,et al. The affected-pedigree-member method of linkage analysis. , 1988, American journal of human genetics.
[20] E S Lander,et al. Homozygosity mapping: a way to map human recessive traits with the DNA of inbred children. , 1987, Science.
[21] E S Lander,et al. Mapping complex genetic traits in humans: new methods using a complete RFLP linkage map. , 1986, Cold Spring Harbor symposia on quantitative biology.
[22] J. Ott. Analysis of Human Genetic Linkage , 1985 .
[23] R. Elston. Genetic Analysis Workshop II: sib pair screening tests for linkage. , 1984, Genetic epidemiology.
[24] H. King,et al. Glucose tolerance and ancestral genetic admixture in six semitraditional pacific populations , 1984, Genetic epidemiology.
[25] K. P. Donnelly,et al. The probability that related individuals share some section of genome identical by descent. , 1983, Theoretical population biology.
[26] K. Isselbacher,et al. Benign recurrent intrahepatic cholestasis. , 1963, Clinical medicine.
[27] W. Summerskill,et al. Benign recurrent intrahepatic "obstructive" jaundice. , 1959, Lancet.