Progress towards completing the human linkage map.
暂无分享,去创建一个
[1] R L White,et al. The CEPH consortium linkage map of human chromosome 1. , 1991, Genomics.
[2] P. Green,et al. Guidelines for human linkage maps: an international system for human linkage maps (ISLM, 1990). , 1991, Genomics.
[3] D. Botstein,et al. 1989 Allen Award address: the American Society of Human Genetics annual meeting, Baltimore. , 1990, American journal of human genetics.
[4] R. White. 1989 Allen Award address: the American Society of Human Genetics annual meeting, Baltimore. , 1990, American journal of human genetics.
[5] N. Arnheim,et al. PCR analysis of DNA sequences in single cells: single sperm gene mapping and genetic disease diagnosis. , 1990, Genomics.
[6] J. Kidd,et al. A refined linkage map for DNA markers around the pericentromeric region of chromosome 10. , 1990, Genomics.
[7] J. C. Stephens,et al. Mapping the human genome: current status. , 1990, Science.
[8] K. Kidd,et al. The human genome map 1990. , 1990, Science.
[9] T. Sekiya,et al. DNA sequence polymorphisms in Alu repeats. , 1990, Genomics.
[10] S. Reeders,et al. Polymorphism in the APNH gene, detected by denaturing gradient gel electrophoresis. , 1990, Nucleic acids research.
[11] J L Haines,et al. A genetic linkage map of chromosome 17. , 1990, Genomics.
[12] J. Weber. Informativeness of human (dC-dA)n.(dG-dT)n polymorphisms. , 1990, Genomics.
[13] L. Lerman,et al. Comprehensive detection of single base changes in human genomic DNA using denaturing gradient gel electrophoresis and a GC clamp. , 1990, Genomics.
[14] K K Kidd,et al. Haplotype of multiple polymorphisms resolved by enzymatic amplification of single DNA molecules. , 1990, Proceedings of the National Academy of Sciences of the United States of America.
[15] K. Kidd,et al. Report of the DNA committee and catalogues of cloned and mapped genes and DNA polymorphisms (Part 1 of 14) , 1990 .
[16] N. Morton,et al. Standard maps of chromosome 10 , 1990, Annals of human genetics.
[17] M. Leppert,et al. Multiple mutations in highly conserved residues are found in mildly affected cystic fibrosis patients , 1990, Cell.
[18] S. Antonarakis,et al. The polydeoxyadenylate tract of Alu repetitive elements is polymorphic in the human genome. , 1990, Proceedings of the National Academy of Sciences of the United States of America.
[19] H. Cann,et al. Centre d'etude du polymorphisme humain (CEPH): collaborative genetic mapping of the human genome. , 1990, Genomics.
[20] H Donis-Keller,et al. The CEPH consortium primary linkage map of human chromosome 10. , 1990, Genomics.
[21] Victoria Wilson,et al. Repeat unit sequence variation in minisatellites: A novel source of DNA polymorphism for studying variation and mutation by single molecule analysis , 1990, Cell.
[22] T. Sekiya,et al. Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction. , 1989, Genomics.
[23] Y. Nakamura,et al. Twenty-eight loci form a continuous linkage map of markers for human chromosome 1. , 1989, Genomics.
[24] K. Kidd,et al. Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms. , 1989, Cytogenetics and cell genetics.
[25] T. Sekiya,et al. Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms. , 1989, Proceedings of the National Academy of Sciences of the United States of America.
[26] J. Weber,et al. Abundant class of human DNA polymorphisms which can be typed using the polymerase chain reaction. , 1989, American journal of human genetics.
[27] M. Litt,et al. A hypervariable microsatellite revealed by in vitro amplification of a dinucleotide repeat within the cardiac muscle actin gene. , 1989, American journal of human genetics.
[28] A. Jeffreys,et al. Clustering of hypervariable minisatellites in the proterminal regions of human autosomes. , 1988, Genomics.
[29] Henry A. Erlich,et al. Amplification and analysis of DNA sequences in single human sperm and diploid cells , 1988, Nature.
[30] M. Daly,et al. A genetic linkage map of the human genome , 1987, Cell.
[31] G M Lathrop,et al. A primary genetic linkage map for human chromosome 12. , 1987, Genomics.
[32] Y. Nakamura,et al. Variable number of tandem repeat (VNTR) markers for human gene mapping. , 1987, Science.
[33] M. Wapenaar,et al. The X chromosome shows less genetic variation at restriction sites than the autosomes. , 1986, American journal of human genetics.
[34] J. Bennett,et al. Novel sex differences in linkage values and meiotic chromosome behaviour in a marsupial , 1986, Nature.
[35] R. White,et al. The genetic linkage map of the human X chromosome. , 1985, Science.
[36] J. Ott. Analysis of Human Genetic Linkage , 1985 .
[37] Swee Lay Thein,et al. Hypervariable ‘minisatellite’ regions in human DNA , 1985, Nature.
[38] K. Davies,et al. Genetic mapping of the human X chromosome by using restriction fragment length polymorphisms. , 1984, Proceedings of the National Academy of Sciences of the United States of America.
[39] R. White,et al. A highly polymorphic locus in human DNA. , 1980, Proceedings of the National Academy of Sciences of the United States of America.
[40] D. Botstein,et al. Construction of a genetic linkage map in man using restriction fragment length polymorphisms. , 1980, American journal of human genetics.
[41] B. Keats,et al. Report of the committee on linkage and gene order. , 1988, Cytogenetics and cell genetics.
[42] K. Kidd,et al. Progress toward resolving the possible linkage of multiple endocrine neoplasia type 2A to haptoglobin and group‐specific loci: Use of restriction fragment length polymorphisms extends exclusion region , 1986, Genetic epidemiology.