Literature DB >> 2738905

Single base pair alterations as the predominant category of mutation in type I osteogenesis imperfecta.

A J Brookes, B Sykes, E Solomon.   

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Year:  1989        PMID： 2738905      PMCID： PMC1015632          DOI： 10.1136/jmg.26.6.410

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


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  5 in total

Review 1.  Osteogenesis imperfecta.

Authors:  W G Cole
Journal:  Baillieres Clin Endocrinol Metab       Date:  1988-02

2.  Type I osteogenesis imperfecta: a nonfunctional allele for pro alpha 1 (I) chains of type I procollagen.

Authors:  G S Barsh; K E David; P H Byers
Journal:  Proc Natl Acad Sci U S A       Date:  1982-06       Impact factor: 11.205

3.  A new method for detection of small modifications in genomic DNA, applied to the human delta-beta globin gene cluster.

Authors:  Y Chebloune; G Trabuchet; D Poncet; M Cohen-Solal; C Faure; G Verdier; V M Nigon
Journal:  Eur J Biochem       Date:  1984-08-01

4.  Diminished type I collagen synthesis and reduced alpha 1(I) collagen messenger RNA in cultured fibroblasts from patients with dominantly inherited (type I) osteogenesis imperfecta.

Authors:  D W Rowe; J R Shapiro; M Poirier; S Schlesinger
Journal:  J Clin Invest       Date:  1985-08       Impact factor: 14.808

5.  Osteogenesis imperfecta is linked to both type I collagen structural genes.

Authors:  B Sykes; D Ogilvie; P Wordsworth; N Jones
Journal:  Lancet       Date:  1986-07-12       Impact factor: 79.321
  5 in total

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