Literature DB >> 11303515

Development and application of linkage analysis in genetic diagnosis of familial hypertrophic cardiomyopathy.

J Mogensen, P S Andersen, U Steffensen, M Christiansen, H Egeblad, N Gregersen, A D Børglum.   

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Year:  2001        PMID： 11303515      PMCID： PMC1734831          DOI： 10.1136/jmg.38.3.193

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


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  2 in total

1.  Idiopathic restrictive cardiomyopathy is part of the clinical expression of cardiac troponin I mutations.

Authors:  Jens Mogensen; Toru Kubo; Mauricio Duque; William Uribe; Anthony Shaw; Ross Murphy; Juan R Gimeno; Perry Elliott; William J McKenna
Journal:  J Clin Invest       Date:  2003-01       Impact factor: 14.808

2.  Setting up Multiplex Panels for Genetic Testing of Familial Hypertrophic Cardiomyopathy Based on Linkage Analysis.

Authors:  Hoorieh Saghafi; Majid Haghjoo; Sima Sabbagh; Niloofar Samiee; Farve Vakilian; Mohammad Taghi Salehi Omran; Masoomeh Dadashi; Ahmad Amin; Mohammad Keramatipour
Journal:  Iran J Public Health       Date:  2016-03       Impact factor: 1.429
  2 in total

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