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Rinsho Byori. the Japanese Journal of Clinical Pathology|March 6, 1999
[Genomic instability and neurodegenerative disease]T Miki, H YamagataNihon Rinsho. Japanese Journal of Clinical Medicine|January 22, 1998
[Molecular genetics of myotonic dystrophy--population genetics of the CTG repeat expansion of the MTPK gene]H Yamagata, T Miki, T OgiharaRinsho Shinkeigaku = Clinical Neurology|December 1, 1995
[Molecular genetics of myotonic dystrophy]T Miki, H Yamagata, T OgiharaRinsho Shinkeigaku = Clinical Neurology|March 1, 1993
[DNA diagnosis of myotonic dystrophy in a family]K Kihara, H Yamagata, T Miki, et al.Nihon Rinsho. Japanese Journal of Clinical Medicine|September 1, 1993
[Advances in molecular genetics of myotonic dystrophy]H Yamagata, N Yamanaka, T Miki, et al.Journal of Human Genetics|December 16, 1998
Further evidence for a major ancient mutation underlying myotonic dystrophy from linkage disequilibrium studies in the Japanese populationH Yamagata, M Nakagawa, K Johnson, et al.Journal of Human Genetics|June 8, 2001
Frequent loss of heterozygosity at 3p25-p26 is associated with invasive oral squamous cell carcinomaH Kayahara, H Yamagata, H Tanioka, et al.Clinical Genetics|November 27, 1998
Molecular analysis of two pre-mutations in myotonic dystrophyH Yamagata, M Kinoshita, T Komori, et al.Pediatric Neurology|May 1, 1997
Haplotype analysis of congenital myotonic dystrophy patients from asymptomatic DM fatherN Tachi, K Ohya, H Yamagata, et al.Human Genetics|February 1, 1996
Association of CTG repeats and the 1-kb Alu insertion/deletion polymorphism at the myotonin protein kinase gene in the Japanese population suggests a common Eurasian origin of the myotonic dystrophy mutationH Yamagata, T Miki, M Nakagawa, et al.Pageof 105