Literature DB >> 1303179

cA479 (D3S719): a cosmid mapped telomeric of the Von Hippel Lindau disease gene contains the D3S18 locus.

W Liu1, J Vance, D I Smith.   

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Year:  1992        PMID: 1303179     DOI: 10.1093/hmg/1.3.201

Source DB:  PubMed          Journal:  Hum Mol Genet        ISSN: 0964-6906            Impact factor:   6.150


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  4 in total

1.  Precise localisation of 3p25 breakpoints in four patients with the 3p-syndrome.

Authors:  T Drumheller; B C McGillivray; D Behrner; P MacLeod; D E McFadden; J Roberson; C Venditti; K Chorney; M Chorney; D I Smith
Journal:  J Med Genet       Date:  1996-10       Impact factor: 6.318

2.  Genetic mapping of dinucleotide repeat polymorphisms and von Hippel-Lindau disease on chromosome 3p25-26.

Authors:  M A Pericak-Vance; K J Nunes; E Whisenant; D B Loeb; K W Small; J M Stajich; J B Rimmler; L H Yamaoka; D I Smith; H A Drabkin
Journal:  J Med Genet       Date:  1993-06       Impact factor: 6.318

3.  Detailed genetic mapping of the von Hippel-Lindau disease tumour suppressor gene.

Authors:  F M Richards; E R Maher; F Latif; M E Phipps; K Tory; M Lush; P A Crossey; B Oostra; P Enblad; K H Gustavson
Journal:  J Med Genet       Date:  1993-02       Impact factor: 6.318

4.  von Hippel-Lindau disease: identification of deletion mutations by pulsed-field gel electrophoresis.

Authors:  M Yao; F Latif; M L Orcutt; I Kuzmin; T Stackhouse; F W Zhou; K Tory; F M Duh; F Richards; E Maher
Journal:  Hum Genet       Date:  1993-12       Impact factor: 4.132

  4 in total

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