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3 in total

1. A frequent HaeIII RFLP of the human fibronectin gene.

Authors: M Colombi; R Gardella; S Barlati; A Vaheri
Journal: Nucleic Acids Res Date: 1987-08-25 Impact factor: 16.971

2. Human fibronectin: cell specific alternative mRNA splicing generates polypeptide chains differing in the number of internal repeats.

Authors: A R Kornblihtt; K Vibe-Pedersen; F E Baralle
Journal: Nucleic Acids Res Date: 1984-07-25 Impact factor: 16.971

3. 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

3 in total

1. Exclusion of stromelysin-1, stromelysin-2, interstitial collagenase and fibronectin genes as the mutant loci in a family with recessive epidermolysis bullosa dystrophica and a form of cerebellar ataxia.

Authors: M Colombi; R Gardella; N Zoppi; L Moro; D Marini; N K Spurr; S Barlati
Journal: Hum Genet Date: 1992-07 Impact factor: 4.132

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. 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

3 in total