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Attitudes towards Preimplantation Genetic Diagnosis - a German and Japanese comparison.

• Authors : Wüstner, Kerstin¹ (AUTHOR) ; Heinze, Ulrich² (AUTHOR)

• Source: New Genetics & Society. Apr2007, Vol. 26 Issue 1, p1-27. 27p. 7 Charts, 8 Graphs.

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Systematic evaluation of personal genome services for Japanese individuals.

• Authors : Kido, Takashi¹; Kawashima, Minae²; Nishino, Seiji³

• Source: Journal of Human Genetics. Nov2013, Vol. 58 Issue 11, p734-741. 8p.

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The novel and independent association between single-point SNP of NPHP4 gene and renal function in non-diabetic Japanese population: the Takahata study.

• Authors : Konta, Tsuneo¹; Takasaki, Satoshi¹; Ichikawa, Kazunobu¹

• Source: Journal of Human Genetics. Dec2010, Vol. 55 Issue 12, p791-795. 5p. 2 Diagrams, 4 Charts.

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The C677T mutation in the methylene tetrahydrofolate reductase gene increases serum uric acid in elderly men.

• Authors : Zuo, M.; Nishio, H.; Lee, M. J.

• Source: Journal of Human Genetics. 2000, Vol. 45 Issue 4, p257. 6p.

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Guidelines for genetic testing. The Japan Society of Human Genetics, Council Committee of Ethics.

• Authors : Matsuda I; Niikawa N; Sato K ...

Subjects: Genetic Diseases, Inborn/Genetic Diseases, Inborn/Genetic Diseases, Inborn/*diagnosis; Ethics, Medical ; Female

• Source: Journal of human genetics [J Hum Genet] 2001; Vol. 46 (3), pp. 163-5.Publisher: Nature Pub. Group Country of Publication: England NLM ID: 9808008 Publication Model: Print Cited Medium: Print ISSN: 1434-5161 (Print)

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Inherited Arrhythmic Disorders in Japan.

• Authors : HIRAOKA, MASAYASU¹ (AUTHOR)

• Source: Journal of Cardiovascular Electrophysiology. Apr2003, Vol. 14 Issue 4, p431-434. 4p. 1 Chart.

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Molecular epidemiology of C9 deficiency heterozygotes with an Arg95Stop mutation of the C9 gene in Japan.

• Authors : Kira, R.; Ihara, Kenji; Watanabe, Kyoko

• Source: Journal of Human Genetics. 1999, Vol. 44 Issue 2, p109. 3p.

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How chemicals can speed up evolution.

• Authors : Coghlan, Andy

• Source: New Scientist. 5/6/2006, Vol. 190 Issue 2550, p16-16. 3/4p.

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The T911C (F304S) substitution in the human ALG6 gene is a common polymorphism and not a causal mutation of CDG-Ic.

• Authors : Vuillaumier-Barrot, Sandrine; Le Bizec, Christiane; Durand, Geneviève

• Source: Journal of Human Genetics. 2001, Vol. 46 Issue 9, p547. 2p.

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ACHILLES' HELIX.

• Authors : Wright, Robert

Subjects: HUMAN genome; SCIENTISTS; HUMAN chromosomesJAPANWATSON, James D., 1928-

• Source: New Republic; 7/9/90 - 7/16/90, Vol. 203 Issue 2/3, p21-31, 10p, 2 Black and White Photographs

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