Literature DB >> 1980487

Direct haplotyping by double digestion of PCR-amplified creatine kinase (CKMM): application to myotonic dystrophy diagnosis.

C Lavedan1, C Duros, D Savoy, S Leblond, J Bailly, R Korneluk, C Junien.   

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Year:  1990        PMID： 1980487     DOI： 10.1016/0888-7543(90)90265-v

Source DB:  PubMed          Journal:  Genomics        ISSN： 0888-7543            Impact factor:   5.736


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  2 in total

1.  A novel NcoI polymorphism creates a fifth haplotype in the 3' untranslated region of CKM.

Authors:  A M Differ; M Bobrow; C G Mathew
Journal:  Hum Genet       Date:  1992-08       Impact factor: 4.132

2.  Linkage disequilibrium detected between myotonic dystrophy and the anonymous marker D19S63 in the Spanish population.

Authors:  A Cobo; D Grinberg; S Balcells; L Vilageliu; R Gonzàlez-Duarte; M Baiget
Journal:  Hum Genet       Date:  1992-05       Impact factor: 4.132
  2 in total

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