Literature DB >> 2892167

Isolation and mapping of a polymorphic DNA sequence pYNH24 on chromosome 2 (D2S44).

Y Nakamura1, S Gillilan, P O'Connell, M Leppert, G M Lathrop, J M Lalouel, R White.   

Abstract

Mesh：

Year:  1987        PMID： 2892167      PMCID： PMC306577          DOI： 10.1093/nar/15.23.10073

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN： 0305-1048            Impact factor:   16.971


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  2 in total

1.  Report of the Committee on the Genetic Constitution of Chromosomes 1 and 2.

Authors:  S Povey; N E Morton; S L Sherman
Journal:  Cytogenet Cell Genet       Date:  1985

2.  Multilocus linkage analysis in humans: detection of linkage and estimation of recombination.

Authors:  G M Lathrop; J M Lalouel; C Julier; J Ott
Journal:  Am J Hum Genet       Date:  1985-05       Impact factor: 11.025
  2 in total
  21 in total

1.  Independence of VNTR alleles defined as fixed bins.

Authors:  B S Weir
Journal:  Genetics       Date:  1992-04       Impact factor: 4.562

2.  An exclusion map for pre-eclampsia: assuming autosomal recessive inheritance.

Authors:  C Hayward; J Livingstone; S Holloway; W A Liston; D J Brock
Journal:  Am J Hum Genet       Date:  1992-04       Impact factor: 11.025

3.  Fixed-bin analysis for statistical evaluation of continuous distributions of allelic data from VNTR loci, for use in forensic comparisons.

Authors:  B Budowle; A M Giusti; J S Waye; F S Baechtel; R M Fourney; D E Adams; L A Presley; H A Deadman; K L Monson
Journal:  Am J Hum Genet       Date:  1991-05       Impact factor: 11.025

4.  A new DNA profiling system for cell line identification for use in cell banks in Japan.

Authors:  M Honma; E Kataoka; K Ohnishi; T Ohno; M Takeuchi; N Nomura; H Mizusawa
Journal:  In Vitro Cell Dev Biol       Date:  1992-01

5.  Identification of complex DNA polymorphisms based on variable number of tandem repeats (VNTR) and restriction site polymorphism.

Authors:  J S Waye; R M Fourney
Journal:  Hum Genet       Date:  1990-02       Impact factor: 4.132

6.  Confirmation of genetic heterogeneity in limb-girdle muscular dystrophy: linkage of an autosomal dominant form to chromosome 5q.

Authors:  M C Speer; L H Yamaoka; J H Gilchrist; C P Gaskell; J M Stajich; J M Vance; A Kazantsev; A A Lastra; C S Haynes; J S Beckmann
Journal:  Am J Hum Genet       Date:  1992-06       Impact factor: 11.025

7.  Minisatellite linkage maps in the mouse by cross-hybridization with human probes containing tandem repeats.

Authors:  C Julier; B de Gouyon; M Georges; J L Guénet; Y Nakamura; P Avner; G M Lathrop
Journal:  Proc Natl Acad Sci U S A       Date:  1990-06       Impact factor: 11.205

8.  Telomere elongation observed in immortalized human fibroblasts by treatment with 60Co gamma rays or 4-nitroquinoline 1-oxide.

Authors:  S Sugihara; K Mihara; T Marunouchi; H Inoue; M Namba
Journal:  Hum Genet       Date:  1996-01       Impact factor: 4.132

9.  Diversity of ethnic and racial VNTR RFLP fixed-bin frequency distributions.

Authors:  J Hartmann; R Keister; B Houlihan; L Thompson; R Baldwin; E Buse; B Driver; M Kuo
Journal:  Am J Hum Genet       Date:  1994-12       Impact factor: 11.025

10.  Trisomy 15 with loss of the paternal 15 as a cause of Prader-Willi syndrome due to maternal disomy.

Authors:  S B Cassidy; L W Lai; R P Erickson; L Magnuson; E Thomas; R Gendron; J Herrmann
Journal:  Am J Hum Genet       Date:  1992-10       Impact factor: 11.025
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