A genetic linkage map of chromosome 17. 1990

J L Haines, and L J Ozelius, and H McFarlane, and A Menon, and S Tzall, and F Martiniuk, and R Hirschhorn, and J F Gusella
Neurogenetics Laboratory, Massachusetts General Hospital, Boston.

We have developed a genetic linkage map of 19 markers (including nine genes) on human chromosome 17, providing 13 reference points along virtually the entire length of this chromosome. The map covers an estimated 149 cM in length (sex-averaged), with a total length of 214 cM in females and 95 cM in males. This sex difference appears to be significant along virtually the entire length of the map. This map will be useful both for providing reference points for fine structure genetic and physical mapping and for genetic linkage studies of diseases, including von Recklinghausen neurofibromatosis and Charcot-Marie-Tooth disease.

UI MeSH Term Description Entries
D008040 Genetic Linkage The co-inheritance of two or more non-allelic GENES due to their being located more or less closely on the same CHROMOSOME. Genetic Linkage Analysis,Linkage, Genetic,Analyses, Genetic Linkage,Analysis, Genetic Linkage,Genetic Linkage Analyses,Linkage Analyses, Genetic,Linkage Analysis, Genetic
D008297 Male Males
D011995 Recombination, Genetic Production of new arrangements of DNA by various mechanisms such as assortment and segregation, CROSSING OVER; GENE CONVERSION; GENETIC TRANSFORMATION; GENETIC CONJUGATION; GENETIC TRANSDUCTION; or mixed infection of viruses. Genetic Recombination,Recombination,Genetic Recombinations,Recombinations,Recombinations, Genetic
D002874 Chromosome Mapping Any method used for determining the location of and relative distances between genes on a chromosome. Gene Mapping,Linkage Mapping,Genome Mapping,Chromosome Mappings,Gene Mappings,Genome Mappings,Linkage Mappings,Mapping, Chromosome,Mapping, Gene,Mapping, Genome,Mapping, Linkage,Mappings, Chromosome,Mappings, Gene,Mappings, Genome,Mappings, Linkage
D002886 Chromosomes, Human, Pair 17 A specific pair of GROUP E CHROMOSOMES of the human chromosome classification. Chromosome 17
D003627 Data Interpretation, Statistical Application of statistical procedures to analyze specific observed or assumed facts from a particular study. Data Analysis, Statistical,Data Interpretations, Statistical,Interpretation, Statistical Data,Statistical Data Analysis,Statistical Data Interpretation,Analyses, Statistical Data,Analysis, Statistical Data,Data Analyses, Statistical,Interpretations, Statistical Data,Statistical Data Analyses,Statistical Data Interpretations
D005260 Female Females
D005819 Genetic Markers A phenotypically recognizable genetic trait which can be used to identify a genetic locus, a linkage group, or a recombination event. Chromosome Markers,DNA Markers,Markers, DNA,Markers, Genetic,Genetic Marker,Marker, Genetic,Chromosome Marker,DNA Marker,Marker, Chromosome,Marker, DNA,Markers, Chromosome
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D012984 Software Sequential operating programs and data which instruct the functioning of a digital computer. Computer Programs,Computer Software,Open Source Software,Software Engineering,Software Tools,Computer Applications Software,Computer Programs and Programming,Computer Software Applications,Application, Computer Software,Applications Software, Computer,Applications Softwares, Computer,Applications, Computer Software,Computer Applications Softwares,Computer Program,Computer Software Application,Engineering, Software,Open Source Softwares,Program, Computer,Programs, Computer,Software Application, Computer,Software Applications, Computer,Software Tool,Software, Computer,Software, Computer Applications,Software, Open Source,Softwares, Computer Applications,Softwares, Open Source,Source Software, Open,Source Softwares, Open,Tool, Software,Tools, Software

Related Publications

J L Haines, and L J Ozelius, and H McFarlane, and A Menon, and S Tzall, and F Martiniuk, and R Hirschhorn, and J F Gusella
May 1989, Genomics,
J L Haines, and L J Ozelius, and H McFarlane, and A Menon, and S Tzall, and F Martiniuk, and R Hirschhorn, and J F Gusella
January 1993, Genomics,
J L Haines, and L J Ozelius, and H McFarlane, and A Menon, and S Tzall, and F Martiniuk, and R Hirschhorn, and J F Gusella
January 1985, Annals of the New York Academy of Sciences,
J L Haines, and L J Ozelius, and H McFarlane, and A Menon, and S Tzall, and F Martiniuk, and R Hirschhorn, and J F Gusella
August 1988, Genomics,
J L Haines, and L J Ozelius, and H McFarlane, and A Menon, and S Tzall, and F Martiniuk, and R Hirschhorn, and J F Gusella
November 1990, Genomics,
J L Haines, and L J Ozelius, and H McFarlane, and A Menon, and S Tzall, and F Martiniuk, and R Hirschhorn, and J F Gusella
January 1993, Genomics,
J L Haines, and L J Ozelius, and H McFarlane, and A Menon, and S Tzall, and F Martiniuk, and R Hirschhorn, and J F Gusella
January 1993, Genomics,
J L Haines, and L J Ozelius, and H McFarlane, and A Menon, and S Tzall, and F Martiniuk, and R Hirschhorn, and J F Gusella
August 1992, Genomics,
J L Haines, and L J Ozelius, and H McFarlane, and A Menon, and S Tzall, and F Martiniuk, and R Hirschhorn, and J F Gusella
March 1990, Genomics,
J L Haines, and L J Ozelius, and H McFarlane, and A Menon, and S Tzall, and F Martiniuk, and R Hirschhorn, and J F Gusella
September 1987, Genomics,
Copied contents to your clipboard!