Literature DB >> 2893345

Isolation and mapping of a polymorphic DNA sequence pMLJ14 on chromosome 14 [D14S13].

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

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Year:  1988        PMID： 2893345      PMCID： PMC334662          DOI： 10.1093/nar/16.1.381

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


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  3 in total

1.  Variable number of tandem repeat (VNTR) markers for human gene mapping.

Authors:  Y Nakamura; M Leppert; P O'Connell; R Wolff; T Holm; M Culver; C Martin; E Fujimoto; M Hoff; E Kumlin
Journal:  Science       Date:  1987-03-27       Impact factor: 47.728

2.  Report of the Committee on the Genetic Constitution of Chromosomes 13, 14, 15 and 16.

Authors:  D R Cox; T Gedde-Dahl
Journal:  Cytogenet Cell Genet       Date:  1985

3.  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
  3 in total
  8 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.  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

3.  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

4.  Molecular characterization of a patient with del(1)(q23-q25).

Authors:  B Franco; L W Lai; D Patterson; D H Ledbetter; B J Trask; G van den Engh; S Iannaccone; S Frances; P I Patel; J R Lupski
Journal:  Hum Genet       Date:  1991-07       Impact factor: 4.132

5.  Molecular analysis redefines three human chromosome 14 deletions.

Authors:  R F Wintle; T Costa; R H Haslam; I E Teshima; D W Cox
Journal:  Hum Genet       Date:  1995-05       Impact factor: 4.132

6.  De novo microdeletion on an inherited Robertsonian translocation chromosome: a cause for dysmorphism in the apparently balanced translocation carrier.

Authors:  D T Bonthron; S J Smith; J Fantes; C M Gosden
Journal:  Am J Hum Genet       Date:  1993-09       Impact factor: 11.025

7.  Maternal uniparental isodisomy of chromosome 14: association with autosomal recessive rod monochromacy.

Authors:  L Pentao; R A Lewis; D H Ledbetter; P I Patel; J R Lupski
Journal:  Am J Hum Genet       Date:  1992-04       Impact factor: 11.025

8.  Down syndrome due to de novo Robertsonian translocation t(14q;21q): DNA polymorphism analysis suggests that the origin of the extra 21q is maternal.

Authors:  M B Petersen; P A Adelsberger; A A Schinzel; F Binkert; G K Hinkel; S E Antonarakis
Journal:  Am J Hum Genet       Date:  1991-09       Impact factor: 11.025
  8 in total

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