A genetic linkage map of the human genome

[1]  K. Kidd,et al.  Report of the committee on human gene mapping by recombinant DNA techniques. , 1988, Cytogenetics and cell genetics.

[2]  R. Lewis.  Gene for von Recklinghausen neurofibromatosis is in the pericentromeric region of chromosome 17 , 1988 .

[3]  T. Farag,et al.  Familial hypercholesterolemia. , 1988, Journal of the Royal Society of Medicine.

[4]  P. D. Smet.  Notes added in proof , 1988, EMBO Journal.

[5]  M. Leppert,et al.  Linkage, physical mapping, and DNA sequence analysis of pseudoautosomal loci on the human X and Y chromosomes. , 1987, Genomics.

[6]  M. Daly,et al.  MAPMAKER: an interactive computer package for constructing primary genetic linkage maps of experimental and natural populations. , 1987, Genomics.

[7]  S. Folstein,et al.  Localization of the huntington's disease gene to a small segment of chromosome 4 flanked by D4S10 and the telomere , 1987, Cell.

[8]  S. H. Rider,et al.  Chromosome 5 allele loss in human colorectal carcinomas , 1987, Nature.

[9]  F. C. Lucibello,et al.  Localization of the gene for familial adenomatous polyposis on chromosome 5 , 1987, Nature.

[10]  K. Kidd,et al.  Assignment of multiple endocrine neoplasia type 2A to chromosome 10 by linkage , 1987, Nature.

[11]  K. Kidd,et al.  Report of the committee on human gene mapping by recombinant DNA techniques. , 1987, Cytogenetics and cell genetics.

[12]  E S Lander,et al.  Homozygosity mapping: a way to map human recessive traits with the DNA of inbred children. , 1987, Science.

[13]  M. Pericak-Vance,et al.  Genetic linkage of von Recklinghausen neurofibromatosis to the nerve growth factor receptor gene , 1987, Cell.

[14]  Y. Nakamura,et al.  Gene for von Recklinghausen neurofibromatosis is in the pericentromeric region of chromosome 17. , 1987, Science.

[15]  Y. Li,et al.  Bgl II RFLP recognized by a human IRBP cDNA localized to chromosome 10. , 1987, Nucleic acids research.

[16]  E. Lander,et al.  Construction of multilocus genetic linkage maps in humans. , 1987, Proceedings of the National Academy of Sciences of the United States of America.

[17]  Y. Nakamura,et al.  Variable number of tandem repeat (VNTR) markers for human gene mapping. , 1987, Science.

[18]  W. Lee,et al.  Human retinoblastoma susceptibility gene: cloning, identification, and sequence , 1987, Science.

[19]  Seashore Mr.  Mendelian Inheritance in Man. Catalogs of Autosomal Dominant, Autosomal Recessive, and X-Linked Phenotypes. 7th Edition. , 1987 .

[20]  D. Pollen,et al.  The genetic defect causing familial Alzheimer's disease maps on chromosome 21. , 1987, Science.

[21]  K. Kidd,et al.  Localization and linkage of three polymorphic DNA sequences on human chromosome 20. , 1987, Cytogenetics and cell genetics.

[22]  C. Mathew,et al.  A linked genetic marker for multiple endocrine neoplasia type 2A on chromosome 10 , 1987, Nature.

[23]  K. Kidd,et al.  Bipolar affective disorders linked to DNA markers on chromosome 11 , 1987, Nature.

[24]  P. Goodfellow,et al.  A pseudoautosomal gene in man. , 1986, Science.

[25]  M. Capecchi,et al.  Introduction of homologous DNA sequences into mammalian cells induces mutations in the cognate gene , 1986, Nature.

[26]  A. Monaco,et al.  Isolation of candidate cDNAs for portions of the Duchenne muscular dystrophy gene , 1986, Nature.

[27]  Stephen H. Friend,et al.  A human DNA segment with properties of the gene that predisposes to retinoblastoma and osteosarcoma , 1986, Nature.

[28]  M. Wapenaar,et al.  The X chromosome shows less genetic variation at restriction sites than the autosomes. , 1986, American journal of human genetics.

[29]  C. A. Smith.  The development of human linkage analysis , 1986, Annals of human genetics.

[30]  J M Lalouel,et al.  A primary genetic map of chromosome 13q. , 1986, American journal of human genetics.

[31]  R. Lothe,et al.  Very close linkage between D2S1 and ACP1 on chromosome 2p , 1986, Annals of human genetics.

[32]  U. Francke,et al.  A variable tandem repeat locus mapped to chromosome band 10q26 is amplified and rearranged in leukocyte DNAs of two cancer patients. , 1986, Nucleic acids research.

[33]  E. Lander,et al.  Strategies for studying heterogeneous genetic traits in humans by using a linkage map of restriction fragment length polymorphisms. , 1986, Proceedings of the National Academy of Sciences of the United States of America.

[34]  R. Martuza,et al.  Loss of genes on chromosome 22 in tumorigenesis of human acoustic neuroma , 1986, Nature.

[35]  H. Willard,et al.  Detection of restriction fragment length polymorphisms at the centromeres of human chromosomes by using chromosome-specific alpha satellite DNA probes: implications for development of centromere-based genetic linkage maps. , 1986, Proceedings of the National Academy of Sciences of the United States of America.

[36]  F. Quan,et al.  Isolation and characterization of the human catalase gene , 1986, Nucleic Acids Res..

[37]  A. Monaco,et al.  Cloning the gene for an inherited human disorder—chronic granulomatous disease—on the basis of its chromosomal location , 1986, Nature.

[38]  N. Morton,et al.  Multipoint linkage analysis. , 1986, American journal of human genetics.

[39]  C. E. Hildebrand,et al.  Human Chromosome–Specific DNA Libraries: Construction and Availability , 1986, Bio/Technology.

[40]  R. White,et al.  Construction of a map of the short arm of human chromosome 6. , 1986, Proceedings of the National Academy of Sciences of the United States of America.

[41]  A. Ross,et al.  Gene transfer and molecular cloning of the human NGF receptor. , 1986, Science.

[42]  J. Weissenbach,et al.  A gradient of sex linkage in the pseudoautosomal region of the human sex chromosomes , 1986, Nature.

[43]  Y. Nakamura,et al.  Construction of human genetic linkage maps: I. Progress and perspectives. , 1986, Cold Spring Harbor symposia on quantitative biology.

[44]  P. Green,et al.  Highly polymorphic RFLP probes as diagnostic tools. , 1986, Cold Spring Harbor symposia on quantitative biology.

[45]  C. Helms,et al.  Factors which equalize the representation of genome segments in recombinant libraries. , 1986, Gene.

[46]  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.

[47]  D. Botstein,et al.  Regional assignments of three polymorphic DNA segments on human chromosome 15 , 1986, Genetic epidemiology.

[48]  L. Tsui,et al.  Cystic Fibrosis Locus Defined by a Genetically Linked Polymorphic Dna Marker Author(s): Lap , 2022 .

[49]  J. Weissenbach,et al.  Pseudoautosomal DNA sequences in the pairing region of the human sex chromosomes , 1985, Nature.

[50]  W. Brown,et al.  Hypervariable telomeric sequences from the human sex chromosomes are pseudoautosomal , 1985, Nature.

[51]  P. Pearson,et al.  An anonymous single copy chromosome 22 clone, D22S10 (22c1-18) identifies an RFLP with PstI. , 1985, Nucleic acids research.

[52]  K. Davies,et al.  A highly polymorphic DNA marker linked to adult polycystic kidney disease on chromosome 16 , 1985, Nature.

[53]  R. White,et al.  A highly polymorphic locus in human DNA revealed by cosmid-derived probes. , 1985, Proceedings of the National Academy of Sciences of the United States of America.

[54]  Davatelis Gn.  Isolation and subregional mapping of an arbitrary cloned probe detecting a common RFLP on human chromosome 2. , 1985 .

[55]  J. Seidman,et al.  Detection of a frequent restriction fragment length polymorphism in the human T cell antigen receptor beta chain locus. A potential diagnostic tool. , 1985, The Journal of clinical investigation.

[56]  K. Kidd,et al.  Linkage analysis of a DNA marker localized to 20p12 and multiple endocrine neoplasia type 2A. , 1985, American journal of human genetics.

[57]  S. Latt,et al.  Two RFLPs identified by a human chromosome #2 clone at 2p15-2p16 (HGM8 assignment no. D2S5). , 1985, Nucleic acids research.

[58]  D. Laurie,et al.  Further studies on bivalent chiasma frequency in human males with normal karyotypes , 1985, Annals of human genetics.

[59]  E. Wijsman,et al.  A systematic approach for detecting high-frequency restriction fragment length polymorphisms using large genomic probes. , 1985, American journal of human genetics.

[60]  D. Laurie,et al.  Further studies on chiasma distribution and interference in the human male , 1985, Annals of human genetics.

[61]  L. Tsui,et al.  Structural and evolutionary relationships among five members of the human gamma-crystallin gene family , 1985, Molecular and cellular biology.

[62]  J. Ott.  Analysis of Human Genetic Linkage , 1985 .

[63]  B. Gallie,et al.  Genetic origin of mutations predisposing to retinoblastoma. , 1985, Science.

[64]  H. Willard,et al.  Isolation of cDNA clones coding for the beta subunit of human beta-hexosaminidase. , 1985, Proceedings of the National Academy of Sciences of the United States of America.

[65]  M. Olson,et al.  A new method for purifying lambda DNA from phage lysates. , 1985, DNA.

[66]  D. Timothy Bishop,et al.  Construction of linkage maps with DNA markers for human chromosomes , 1985, Nature.

[67]  Michael Dean,et al.  A closely linked genetic marker for cystic fibrosis , 1985, Nature.

[68]  G. Davatelis.  Isolation and subregional mapping of an arbitrary cloned probe detecting a common RFLP on human chromosome 2. , 1985, American journal of human genetics.

[69]  Peter J. Scambler,et al.  Localization of cystic fibrosis locus to human chromosome 7cen–q22 , 1985, Nature.

[70]  L. Tsui,et al.  A polymorphic DNA marker linked to cystic fibrosis is located on chromosome 7 , 1985, Nature.

[71]  T. Holm,et al.  A locus on chromosome 11p with multiple restriction site polymorphisms. , 1984, American journal of human genetics.

[72]  D. Botstein,et al.  Occurrence of a transposition from the X-chromosome long arm to the Y-chromosome short arm during human evolution , 1984, Nature.

[73]  C. Cooper,et al.  Molecular cloning of a new transforming gene from a chemically transformed human cell line , 1984, Nature.

[74]  D. Ledbetter,et al.  Organization of the HPRT gene and related sequences in the human genome , 1984, Somatic cell and molecular genetics.

[75]  D. M. Carlson,et al.  Clones from the human gene complex coding for salivary proline-rich proteins. , 1984, Proceedings of the National Academy of Sciences of the United States of America.

[76]  S. O’Brien,et al.  Chromosomal organization of the human dihydrofolate reductase genes: dispersion, selective amplification, and a novel form of polymorphism. , 1984, Proceedings of the National Academy of Sciences of the United States of America.

[77]  J. Chirgwin,et al.  Human renin gene: structure and sequence analysis. , 1984, Proceedings of the National Academy of Sciences of the United States of America.

[78]  J. Ott,et al.  Strategies for multilocus linkage analysis in humans. , 1984, Proceedings of the National Academy of Sciences of the United States of America.

[79]  A. Feinberg,et al.  Somatic deletion and duplication of genes on chromosome 11 in Wilms' tumours , 1984, Nature.

[80]  D. Robertson.  Different Frequency in the Recovery of Crossover Products from Male and Female Gametes of Plants Hypoploid for B-a Translocations in Maize. , 1984, Genetics.

[81]  C. L. Jackson,et al.  Isolation and sequence of a human apolipoprotein CII cDNA clone and its use to isolate and map to human chromosome 19 the gene for apolipoprotein CII. , 1984, Proceedings of the National Academy of Sciences of the United States of America.

[82]  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.

[83]  T. Shows,et al.  DNA polymorphic loci mapped to human chromosomes 3, 5, 9, 11, 17, 18, and 22. , 1984, Proceedings of the National Academy of Sciences of the United States of America.

[84]  P Chambon,et al.  Sequence of the pS2 mRNA induced by estrogen in the human breast cancer cell line MCF-7. , 1984, Nucleic acids research.

[85]  D. Barker,et al.  Restriction sites containing CpG show a higher frequency of polymorphism in human DNA , 1984, Cell.

[86]  T. Mohandas,et al.  Isolation and regional localization of DNA segments revealing polymorphic loci from human chromosome 13. , 1984, American journal of human genetics.

[87]  M. Reitz,et al.  Transformation of NIH 3T3 cells by a human c-sis cDNA clone , 1984, Nature.

[88]  R. A. Swift,et al.  Double cos site vectors: simplified cosmid cloning. , 1983, Gene.

[89]  A. Young,et al.  A polymorphic DNA marker genetically linked to Huntington's disease , 1983, Nature.

[90]  T. Shows,et al.  High-resolution chromosomal localization of human genes for amylase, proopiomelanocortin, somatostatin, and a DNA fragment (D3S1) by in situ hybridization. , 1983, Proceedings of the National Academy of Sciences of the United States of America.

[91]  D. Prockop,et al.  Restriction fragment length polymorphism associated with the pro alpha 2(I) gene of human type I procollagen. Application to a family with an autosomal dominant form of osteogenesis imperfecta. , 1983, The Journal of clinical investigation.

[92]  D. Hogness,et al.  Chromosomal walking and jumping to isolate DNA from the Ace and rosy loci and the bithorax complex in Drosophila melanogaster. , 1983, Journal of molecular biology.

[93]  E. Prochownik,et al.  Isolation of a cDNA clone for human antithrombin III. , 1983, The Journal of biological chemistry.

[94]  L. Leinwand,et al.  Isolation and characterization of human myosin heavy chain genes. , 1983, Proceedings of the National Academy of Sciences of the United States of America.

[95]  K. Davies,et al.  Linkage analysis of two cloned DNA sequences flanking the Duchenne muscular dystrophy locus on the short arm of the human X chromosome. , 1983, Nucleic acids research.

[96]  J. Davide,et al.  Selective amplification of polymorphic dihydrofolate reductase gene loci in Chinese hamster lung cells. , 1982, Proceedings of the National Academy of Sciences of the United States of America.

[97]  H. Willard,et al.  Report of the committee on human gene mapping by recombinant DNA techniques. , 1982, Birth defects original article series.

[98]  Y. Groner,et al.  Human cytoplasmic superoxide dismutase cDNA clone: a probe for studying the molecular biology of Down syndrome. , 1982, Proceedings of the National Academy of Sciences of the United States of America.

[99]  D. Laurie,et al.  Chiasma derived genetic maps and recombination fractions: chromosome 1 , 1982, Annals of human genetics.

[100]  U. Francke,et al.  Assignment of first random restriction fragment length polymorphism (RFLP) locus ((D14S1) to a region of human chromosome 14. , 1982, American journal of human genetics.

[101]  M. Radman,et al.  Radiation-induced base substitution mutagenesis in single-stranded DNA phage M13 , 1981, Nature.

[102]  S. Goodbourn,et al.  Highly variable regions of DNA flank the human alpha globin genes. , 1981, Nucleic acids research.

[103]  W. Rutter,et al.  Polymorphic DNA region adjacent to the 5' end of the human insulin gene. , 1981, Proceedings of the National Academy of Sciences of the United States of America.

[104]  D. Ish-Horowicz,et al.  Rapid and efficient cosmid cloning , 1981, Nucleic Acids Res..

[105]  E. Reddy,et al.  Abelson murine leukemia virus: molecular cloning of infectious integrated proviral DNA. , 1981, Proceedings of the National Academy of Sciences of the United States of America.

[106]  A. F. Scott,et al.  Prenatal diagnosis of sickle cell anemia by restriction and endonuclease analysis: HindIII polymorphisms in gamma-globin genes extend test applicability. , 1980, Proceedings of the National Academy of Sciences of the United States of America.

[107]  D. Housman,et al.  Isolation and localization of DNA segments from specific human chromosomes. , 1980, Proceedings of the National Academy of Sciences of the United States of America.

[108]  D. Botstein,et al.  Construction of a genetic linkage map in man using restriction fragment length polymorphisms. , 1980, American journal of human genetics.

[109]  E. Solomon,et al.  EVOLUTION OF SICKLE VARIANT GENE , 1979, The Lancet.

[110]  T. Maniatis,et al.  The isolation and characterization of linked δ- and β-globin genes from a cloned library of human DNA , 1978, Cell.

[111]  D. Lindsley,et al.  The genetic analysis of meiosis in female Drosophila melanogaster. , 1977, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

[112]  B. Bainbridge,et al.  Genetics , 1981, Experientia.

[113]  D. C. Rao,et al.  An inferred chiasma map of Drosophila melanogaster , 1976, Heredity.

[114]  C. C. Chang,et al.  The interaction of knobs and B chromosomes of maize in determining the level of recombination. , 1974, Genetics.

[115]  V. McKusick.  Mendelian Inheritance in Man: Catalogs of Autosomal Dominant, Autosomal Recessive, and X-Linked Phenotypes , 1983 .

[116]  J. Renwick,et al.  Male and female recombination fractions for the nail‐patella: ABO linkage in man , 1965 .

[117]  Y. Tazima.  The genetics of the silkworm , 1964 .

[118]  N. Morton.  Sequential tests for the detection of linkage. , 1955, American journal of human genetics.

[119]  A. Sturtevant,et al.  THE HISTORY OF GENETICS , 1954 .

[120]  J. Mohr.  A study of linkage in man , 1954 .

[121]  M. Rhoades.  Different Rates of Crossing over in Male and Female Gametes of Maize 1 , 1941 .

[122]  T. Maeda.  Chiasma Studies in the Silkworm, Bombyx mori L , 1939 .

[123]  C. Bridges.  THE RELATION OF THE AGE OF THE FEMALE TO CROSSING OVER IN THE THIRD CHROMOSOME OF DROSOPHILA MELANOGASTER , 1927, The Journal of general physiology.

[124]  T. Morgan.  No crossing-over in the male of Drosophila of genes in the second and third pairs of chromosomes , 1914 .

[125]  A. Sturtevant,et al.  THE LINEAR ARRANGEMENT OF SIX SEX-LINKED FACTORS IN DROSOPHILA, AS SHOWN BY THEIR MODE OF ASSOCIATION , 1913 .

[126]  Highly variable regions of DNA flank the human a globin genes , 2022 .