Literature DB >> 2888087

A frequent HaeIII RFLP of the human fibronectin gene.

M Colombi, R Gardella, S Barlati, A Vaheri.   

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Year:  1987        PMID： 2888087      PMCID： PMC306161          DOI： 10.1093/nar/15.16.6761

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


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  1 in total

1.  In situ localization of human fibronectin (FN) genes to chromosome regions 2p14----p16, 2q34----q36, and 11q12.1----q13.5 in germ line cells, but to chromosome 2 sites only in somatic cells.

Authors:  S C Jhanwar; J T Jensen; M Kaelbling; R S Chaganti; H P Klinger
Journal:  Cytogenet Cell Genet       Date:  1986
  1 in total
  4 in total

1.  Waardenburg syndrome (WS): the analysis of a single family with a WS1 mutation showing linkage to RFLP markers on human chromosome 2q.

Authors:  J H Asher; R Morell; T B Friedman
Journal:  Am J Hum Genet       Date:  1991-01       Impact factor: 11.025

2.  Waardenburg syndrome (WS) type I is caused by defects at multiple loci, one of which is near ALPP on chromosome 2: first report of the WS consortium.

Authors:  L A Farrer; K M Grundfast; J Amos; K S Arnos; J H Asher; P Beighton; S R Diehl; J Fex; C Foy; T B Friedman
Journal:  Am J Hum Genet       Date:  1992-05       Impact factor: 11.025

3.  A common MspI RFLP of the human fibronectin gene (FN1).

Authors:  R Gardella; M Colombi; S Barlati
Journal:  Nucleic Acids Res       Date:  1988-02-25       Impact factor: 16.971

4.  Human fibronectin gene (FN1) RFLPs: mapping and linkage disequilibrium analysis.

Authors:  R Gardella; M Colombi; S Barlati
Journal:  Hum Genet       Date:  1993-12       Impact factor: 4.132
  4 in total

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