Literature DB >> 2073845

Report of the DNA committee and catalogues of cloned and mapped genes and DNA polymorphisms.

R Williamson, A Bowcock, K Kidd, P Pearson, J Schmidtke, H S Chan, M Chipperfield, D N Cooper, J Hewitt, F Lewitter.   

Abstract

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Year:  1990        PMID： 2073845     DOI： 10.1159/000133027

Source DB:  PubMed          Journal:  Cytogenet Cell Genet        ISSN： 0301-0171


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  19 in total

1.  Highly informative dinucleotide repeat polymorphism at the D11S29 locus on chromosome 11q23.

Authors:  L Warnich; I Groenewald; L Theart; A E Retief
Journal:  Hum Genet       Date:  1992-05       Impact factor: 4.132

2.  RsaI RFLP for electron transport flavoprotein-beta(ETFB).

Authors:  V Royal; M J Alberts; M A Pericak-Vance; G Finocchiaro; J Bebout; L Yamaoka; W Y Hung; P C Gaskell; A D Roses
Journal:  Nucleic Acids Res       Date:  1991-07-25       Impact factor: 16.971

3.  Tetranucleotide repeat polymorphism at the HPRT locus.

Authors:  C M Hearne; J A Todd
Journal:  Nucleic Acids Res       Date:  1991-10-11       Impact factor: 16.971

4.  Trinucleotide repeat polymorphism at the CRYG1 locus.

Authors:  C M Hearne; J A Todd
Journal:  Nucleic Acids Res       Date:  1991-10-11       Impact factor: 16.971

5.  The gene responsible for X-linked cleft palate (CPX) in a British Columbia native kindred is localized between PGK1 and DXYS1.

Authors:  S M Gorski; K J Adams; P H Birch; J M Friedman; P J Goodfellow
Journal:  Am J Hum Genet       Date:  1992-05       Impact factor: 11.025

6.  A cluster of highly polymorphic dinucleotide repeats in intron 17b of the cystic fibrosis transmembrane conductance regulator (CFTR) gene.

Authors:  J Zielenski; D Markiewicz; F Rininsland; J Rommens; L C Tsui
Journal:  Am J Hum Genet       Date:  1991-12       Impact factor: 11.025

7.  Genetic screening to identify the gene carrier in Italian and German kindreds affected by multiple endocrine neoplasia type 1 (MEN 1) syndrome.

Authors:  A Morelli; A Falchetti; R Castello; L Furlani; P Tomassetti; F Tonelli; A Frilling; M Serio; M L Brandi
Journal:  J Endocrinol Invest       Date:  1995-05       Impact factor: 4.256

8.  Uniparental disomy occurs infrequently in Wilms tumor patients.

Authors:  P Grundy; B Wilson; P Telzerow; W Zhou; M C Paterson
Journal:  Am J Hum Genet       Date:  1994-02       Impact factor: 11.025

9.  Isolation and mapping of polymorphic cosmid clones used for sublocalization of the multiple endocrine neoplasia type 1 (MEN1) locus.

Authors:  C Larsson; G Weber; E Kvanta; K Lewis; M Janson; C Jones; T Glaser; G Evans; M Nordenskjöld
Journal:  Hum Genet       Date:  1992-05       Impact factor: 4.132

Review 10.  Detection of cryptic chromosomal abnormalities in unexplained mental retardation: a general strategy using hypervariable subtelomeric DNA polymorphisms.

Authors:  A O Wilkie
Journal:  Am J Hum Genet       Date:  1993-09       Impact factor: 11.025
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