A genetic linkage map of 17 markers on human chromosome 21.

[1]  Y. Nakamura,et al.  Twenty-eight loci form a continuous linkage map of markers for human chromosome 1. , 1989, Genomics.

[2]  Y. Nakamura,et al.  A mapped set of genetic markers for human chromosome 9. , 1988, Genomics.

[3]  Y. Nakamura,et al.  A mapped set of DNA markers for human chromosome 15. , 1988, Genomics.

[4]  G. D. Stewart,et al.  Genetic linkage map of human chromosome 21. , 1988, Genomics.

[5]  R. Nussbaum,et al.  Report of the committee on the genetic constitution of the X chromosome. , 1988, Cytogenetics and cell genetics.

[6]  Y. Nakamura,et al.  A primary map of ten DNA markers and two serological markers for human chromosome 19. , 1988, Genomics.

[7]  A. Chakravarti,et al.  Risk of dementia in relatives of patients with Alzheimer's disease , 1988, Neurology.

[8]  Y. Nakamura,et al.  A mapped set of DNA markers for human chromosome 17. , 1988, Genomics.

[9]  R. Timpl,et al.  Cloning and chromosomal localization of human genes encoding the three chains of type VI collagen. , 1988, American journal of human genetics.

[10]  G. Lathrop,et al.  Efficient computations in multilocus linkage analysis. , 1988, American journal of human genetics.

[11]  K. Buetow,et al.  Pairwise linkage analysis of 11 loci on human chromosome 4. , 1988, American journal of human genetics.

[12]  K. Davis,et al.  Familial aggregation in Alzheimer's disease , 1988, Neurology.

[13]  J M Lalouel,et al.  A primary genetic map of markers of human chromosome 10. , 1988, Genomics.

[14]  S. M. Sumi,et al.  Familial alzheimer's disease in american descendants of the volga germans: Probable genetic founder effect , 1988, Annals of neurology.

[15]  D. Price,et al.  β-Amyloid gene is not present in three copies in autopsy-validated Alzheimer's disease , 1987 .

[16]  M. Daly,et al.  A genetic linkage map of the human genome , 1987, Cell.

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

[18]  J. Haines,et al.  The genetic defect in familial Alzheimer's disease is not tightly linked to the amyloid β-protein gene , 1987, Nature.

[19]  G M Lathrop,et al.  A primary genetic linkage map for human chromosome 12. , 1987, Genomics.

[20]  A. Chakravarti,et al.  Evidence for reduced recombination on the nondisjoined chromosomes 21 in Down syndrome. , 1987, Science.

[21]  K H Buetow,et al.  Multipoint gene mapping using seriation. I. General methods. , 1987, American journal of human genetics.

[22]  K H Buetow,et al.  Multipoint gene mapping using seriation. II. Analysis of simulated and empirical data. , 1987, American journal of human genetics.

[23]  G. Scherer,et al.  Anonymous DNA sequence from chromosome 21 showing a three allele insertion/deletion RFLP (HGM 9 provisional no. D21S82) , 1987, Nucleic Acids Res..

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

[25]  K. Davis,et al.  Alzheimer's disease. Morbid risk among first-degree relatives approximates 50% by 90 years of age. , 1987, Archives of general psychiatry.

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

[27]  D. Levanon,et al.  Genomic clones of the human liver-type phosphofructokinase. , 1986, Biochemical and biophysical research communications.

[28]  J. Dausset.  [The Center for the Study of Human Polymorphism]. , 1986, Presse medicale.

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

[30]  E. Jabs,et al.  Regional localization of DNA sequences on chromosome 21 using somatic cell hybrids. , 1986, American journal of human genetics.

[31]  R. White,et al.  The genetic linkage map of the human X chromosome. , 1985, Science.

[32]  G. Landes,et al.  Isolation of polymorphic DNA segments from human chromosome 21. , 1985, Nucleic acids research.

[33]  A. Chakravarti,et al.  A linkage map of three anonymous human DNA fragments and SOD‐1 on chromosome 21. , 1985, The EMBO journal.

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

[35]  N E Morton,et al.  Report of the Committee on Methods of Linkage Analysis and Reporting. , 1985, Cytogenetics and cell genetics.

[36]  G. D. Stewart,et al.  Cloned DNA probes regionally mapped to human chromosome 21 and their use in determining the origin of nondisjunction. , 1985, Nucleic acids research.

[37]  O. Stein,et al.  Architecture and anatomy of the chromosomal locus in human chromosome 21 encoding the Cu/Zn superoxide dismutase. , 1985, The EMBO journal.

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

[39]  A. Feinberg,et al.  A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity. , 1983, Analytical biochemistry.

[40]  P. Chambon,et al.  Cloning of cDNA sequences of hormone-regulated genes from the MCF-7 human breast cancer cell line. , 1982, Nucleic acids research.

[41]  K. Lange,et al.  How many polymorphic genes will it take to span the human genome? , 1982, American journal of human genetics.

[42]  V. Anderson,et al.  Dementia of the Alzheimer Type: Clinical Genetics, Natural History, and Associated Conditions , 1981 .

[43]  J. Ott,et al.  A simple scheme for the analysis of HLA linkages in pedigrees , 1978, Annals of human genetics.

[44]  J. Korenberg,et al.  Base ratio, DNA content, and quinacrine-brightness of human chromosomes. , 1978, Proceedings of the National Academy of Sciences of the United States of America.

[45]  E. Southern.  Detection of specific sequences among DNA fragments separated by gel electrophoresis. , 1975, Journal of molecular biology.

[46]  J. H. Edwards,et al.  The analysis of X‐linkage , 1971, Annals of human genetics.

[47]  B. Carritt,et al.  Report of the committee on the genetic constitution of chromosomes 20, 21, and 22. , 1987, Cytogenetics and cell genetics.

[48]  N. Morton,et al.  Report of the committee on the genetic-constitution of chromosomes 1 and 2. , 1987, Cytogenetics and cell genetics.

[49]  G. D. Stewart,et al.  Human chromosome 21-encoded cDNA clones. , 1986, Gene.

[50]  J. Dausset.  Le centre d'étude du polymorphisme humain. , 1986 .

[51]  P. Jacobs,et al.  Trisomy in man. , 1984, Annual review of genetics.

[52]  B. S. Baker,et al.  The genetic control of meiosis. , 1976, Annual review of genetics.

[53]  D. D. Kosambi.  The estimation of map distances from recombination values. , 1943 .