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J Nakura

Showing results (21-30 of 59) with videos related to

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Nihon Ronen Igakkai Zasshi. Japanese Journal of Geriatrics|December 1, 1995
[Genetic analysis of Werner syndrome in a family]A Morishima, N Mitsuda, J Nakura, et al.
Rinsho Byori. the Japanese Journal of Clinical Pathology|November 1, 1985
[Genetic analysis of hereditary diseases using PFLPs of DNA base sequence]T Miki, J Nakura, Y Kumahara, et al.
The Japanese Journal of Human Genetics|June 1, 1996
Two dinucleotide repeat polymorphisms at the D8S1444 and D8S1445 lociJ Nakura, L Ye, A Takahashi-Fujii, et al.
The Japanese Journal of Human Genetics|June 1, 1995
Dinucleotide repeat polymorphism at the D8S1054N Mitsuda, J Nakura, L Ye, et al.
The Japanese Journal of Human Genetics|December 1, 1994
Dinucleotide repeat polymorphism at the D8S1053J Nakura, L Ye, N Mitsuda, et al.
Lancet (London, England)|April 18, 1992
Homozygosity mapping and Werner's syndromeG D Schellenberg, G M Martin, E M Wijsman, et al.
Genomics|January 1, 1990
The locus for Japanese myotonic dystrophy is also linked to D19S19 on the long arm of chromosome 19Y Takemoto, T Miki, K Nishikawa, et al.
Endocrinologia Japonica|October 1, 1990
A case of first trimester prenatal diagnosis of 21-hydroxylase deficiency with human complement C4 cDNA probeJ Nakura, T Miki, K Nishikawa, et al.
Jinrui Idengaku Zasshi. the Japanese Journal of Human Genetics|December 1, 1990
Mapping of the genes around MEN2A locus using pulsed-field gel electrophoresisN Tanaka, T Miki, M Yamamoto, et al.
Nihon Ronen Igakkai Zasshi. Japanese Journal of Geriatrics|October 14, 2000
[A very elderly autopsy case of cecal cancer with pulmonary lymphangitis carcinomatosa]M Matsubara, K Kohara, K Uemura, et al.
Pageof 6

Showing results (21-30 of 59) with videos related to

Sort By:
Pageof 6
Nihon Ronen Igakkai Zasshi. Japanese Journal of Geriatrics|December 1, 1995
[Genetic analysis of Werner syndrome in a family]A Morishima, N Mitsuda, J Nakura, et al.
Rinsho Byori. the Japanese Journal of Clinical Pathology|November 1, 1985
[Genetic analysis of hereditary diseases using PFLPs of DNA base sequence]T Miki, J Nakura, Y Kumahara, et al.
The Japanese Journal of Human Genetics|June 1, 1996
Two dinucleotide repeat polymorphisms at the D8S1444 and D8S1445 lociJ Nakura, L Ye, A Takahashi-Fujii, et al.
The Japanese Journal of Human Genetics|June 1, 1995
Dinucleotide repeat polymorphism at the D8S1054N Mitsuda, J Nakura, L Ye, et al.
The Japanese Journal of Human Genetics|December 1, 1994
Dinucleotide repeat polymorphism at the D8S1053J Nakura, L Ye, N Mitsuda, et al.
Lancet (London, England)|April 18, 1992
Homozygosity mapping and Werner's syndromeG D Schellenberg, G M Martin, E M Wijsman, et al.
Genomics|January 1, 1990
The locus for Japanese myotonic dystrophy is also linked to D19S19 on the long arm of chromosome 19Y Takemoto, T Miki, K Nishikawa, et al.
Endocrinologia Japonica|October 1, 1990
A case of first trimester prenatal diagnosis of 21-hydroxylase deficiency with human complement C4 cDNA probeJ Nakura, T Miki, K Nishikawa, et al.
Jinrui Idengaku Zasshi. the Japanese Journal of Human Genetics|December 1, 1990
Mapping of the genes around MEN2A locus using pulsed-field gel electrophoresisN Tanaka, T Miki, M Yamamoto, et al.
Nihon Ronen Igakkai Zasshi. Japanese Journal of Geriatrics|October 14, 2000
[A very elderly autopsy case of cecal cancer with pulmonary lymphangitis carcinomatosa]M Matsubara, K Kohara, K Uemura, et al.
Pageof 6