Literature DB >> 2562821

Lack of linkage disequilibrium between two common restriction sites associated with the COLIA2 gene.

S Halloran-Blanton, R C Schwartz, P Tsipouras.   

Abstract

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Year:  1989        PMID： 2562821      PMCID： PMC1715474     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN： 0002-9297            Impact factor:   11.025


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  5 in total

1.  Restriction fragment length polymorphism associated with the pro alpha 2(I) gene of human type I procollagen. Application to a family with an autosomal dominant form of osteogenesis imperfecta.

Authors:  P Tsipouras; J C Myers; F Ramirez; D J Prockop
Journal:  J Clin Invest       Date:  1983-10       Impact factor: 14.808

2.  Use of molecular haplotypes specific for the human pro alpha 2(I) collagen gene in linkage analysis of the mild autosomal dominant forms of osteogenesis imperfecta.

Authors:  C T Falk; R C Schwartz; F Ramirez; P Tsipouras
Journal:  Am J Hum Genet       Date:  1986-03       Impact factor: 11.025

3.  Molecular heterogeneity in the mild autosomal dominant forms of osteogenesis imperfecta.

Authors:  P Tsipouras; A L Børresen; L A Dickson; K Berg; D J Prockop; F Ramirez
Journal:  Am J Hum Genet       Date:  1984-11       Impact factor: 11.025

4.  Detection of a high frequency RsaI polymorphism in the human pro alpha 2(I) collagen gene which is linked to an autosomal dominant form of osteogenesis imperfecta.

Authors:  A F Grobler-Rabie; G Wallis; D K Brebner; P Beighton; A J Bester; C G Mathew
Journal:  EMBO J       Date:  1985-07       Impact factor: 11.598

5.  Sequence diversity within a subgroup of mouse immunoglobulin kappa chains controlled by the IgK-Ef2 locus.

Authors:  C Lazure; W T Hum; D M Gibson
Journal:  J Exp Med       Date:  1981-07-01       Impact factor: 14.307
  5 in total

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