Literature DB >> 2898762

Isolation and mapping of a polymorphic DNA sequence (pCMM6) on chromosome 20 [D20S19].

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

Abstract

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Year:  1988        PMID： 2898762      PMCID： PMC336756          DOI： 10.1093/nar/16.11.5222

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 20, 21, and 22.

Authors:  P Tippett; J C Kaplan
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
  3 in total

1.  Confirmation of linkage of benign familial neonatal convulsions to D20S19 and D20S20.

Authors:  A Malafosse; M Leboyer; O Dulac; Y Navelet; P Plouin; C Beck; H Laklou; G Mouchnino; P Grandscene; L Vallee
Journal:  Hum Genet       Date:  1992-04       Impact factor: 4.132

2.  Benign familial neonatal convulsions: confirmation of genetic heterogeneity and further evidence for a second locus on chromosome 8q.

Authors:  O Steinlein; V Schuster; C Fischer; M Häussler
Journal:  Hum Genet       Date:  1995-04       Impact factor: 4.132

3.  Somatic mosaicism for a newly identified splice-site mutation in a patient with adenosine deaminase-deficient immunodeficiency and spontaneous clinical recovery.

Authors:  R Hirschhorn; D R Yang; A Israni; M L Huie; D R Ownby
Journal:  Am J Hum Genet       Date:  1994-07       Impact factor: 11.025
  3 in total

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