Literature DB >> 2899879

Isolation and mapping of a polymorphic DNA sequence (pMCOC12) on chromosome 14 [D14S20].

Y Nakamura1, M Carlson, E Fujimoto, P O'Connell, M Leppert, G M Lathrop, J M Lalouel, R White.   

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Year:  1988        PMID： 2899879      PMCID： PMC336892          DOI： 10.1093/nar/16.13.6257

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


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  1 in total

1.  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
  1 in total
  3 in total

1.  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

2.  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

3.  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
  3 in total

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