Literature DB >> 3664638

A genetic linkage map of the human genome.

H Donis-Keller1, P Green, C Helms, S Cartinhour, B Weiffenbach, K Stephens, T P Keith, D W Bowden, D R Smith, E S Lander.   

Abstract

We report the construction of a linkage map of the human genome, based on the pattern of inheritance of 403 polymorphic loci, including 393 RFLPs, in a panel of DNAs from 21 three-generation families. By a combination of mathematical linkage analysis and physical localization of selected clones, it was possible to arrange these loci into linkage groups representing 23 human chromosomes. We estimate that the linkage map is detectably linked to at least 95% of the DNA in the human genome.

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Year:  1987        PMID: 3664638     DOI: 10.1016/0092-8674(87)90158-9

Source DB:  PubMed          Journal:  Cell        ISSN: 0092-8674            Impact factor:   41.582


  195 in total

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Authors:  Suzanne M Leal
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2.  Molecular-cytogenetic detection of a deletion of 1p36.3.

Authors:  F Giraudeau; D Aubert; I Young; S Horsley; S Knight; L Kearney; G Vergnaud; J Flint
Journal:  J Med Genet       Date:  1997-04       Impact factor: 6.318

3.  Monte Carlo simulations on marker grouping and ordering.

Authors:  J Wu; J Jenkins; J Zhu; J McCarty; C Watson
Journal:  Theor Appl Genet       Date:  2003-05-22       Impact factor: 5.699

Review 4.  Hot and cold spots of recombination in the human genome: the reason we should find them and how this can be achieved.

Authors:  Norman Arnheim; Peter Calabrese; Magnus Nordborg
Journal:  Am J Hum Genet       Date:  2003-05-22       Impact factor: 11.025

5.  Framework multipoint map of the long arm of human chromosome 4 and telomeric localization of the gene for FSHD.

Authors:  B Weiffenbach; R G Bagley; K Falls; J Dubois; C Hyser; D Storvick; P Schultz; J R Mendell; E C Milner; S J Jacobsen
Journal:  Mamm Genome       Date:  1992       Impact factor: 2.957

6.  A genetic etiology for DiGeorge syndrome: consistent deletions and microdeletions of 22q11.

Authors:  D A Driscoll; M L Budarf; B S Emanuel
Journal:  Am J Hum Genet       Date:  1992-05       Impact factor: 11.025

7.  A hypervariable minisatellite locus D20S73 (pMS214.2) is located on 20q.

Authors:  N J Royle; I Patel; A J Jeffreys
Journal:  Nucleic Acids Res       Date:  1992-03-11       Impact factor: 16.971

8.  A new TaqI allele detected by the CRI-R227 (D4S101) probe in Pima Indians.

Authors:  M G Choi; M Prochazka; P Thuillez; S Lillioja
Journal:  Nucleic Acids Res       Date:  1992-03-11       Impact factor: 16.971

9.  Loss of heterozygosity on chromosome 1q in human breast cancer.

Authors:  L C Chen; C Dollbaum; H S Smith
Journal:  Proc Natl Acad Sci U S A       Date:  1989-09       Impact factor: 11.205

10.  Type 2 NF1 deletions are highly unusual by virtue of the absence of nonallelic homologous recombination hotspots and an apparent preference for female mitotic recombination.

Authors:  Katharina Steinmann; David N Cooper; Lan Kluwe; Nadia A Chuzhanova; Cornelia Senger; Eduard Serra; Conxi Lazaro; Montserrat Gilaberte; Katharina Wimmer; Viktor-Felix Mautner; Hildegard Kehrer-Sawatzki
Journal:  Am J Hum Genet       Date:  2007-10-31       Impact factor: 11.025

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