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Nonparametric estimation of LOH using Affymetrix SNP genotyping arrays for unpaired samples

Journal of Human Genetics, 2008, Vol.53(11), pp.983-990 [Peer Reviewed Journal]

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Mitochondrial disorders

Japanese Journal of Human Genetics, 1997, Vol.42(4), pp.473-487 [Peer Reviewed Journal]

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Carrier frequency of GJB2 (connexin-26) mutations causing inherited deafness in the Korean population

Journal of Human Genetics, 2008, Vol.53(11-12), pp.1022-1028 [Peer Reviewed Journal]

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Association study of the C3 gene with adult and childhood asthma

Journal of Human Genetics, 2008, Vol.53(8), pp.728-738 [Peer Reviewed Journal]

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G6PD deficiency assessment in Freetown, Sierra Leone, reveals further insight into the molecular heterogeneity of G6PD A-.

Journal of human genetics, 2008, Vol.53(7), pp.675-679 [Peer Reviewed Journal]

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Association study to evaluate the serotonin transporter and apolipoprotein E genes in frontotemporal lobar degeneration in Italy.

Journal of human genetics, 2008, Vol.53(11-12), pp.1029-1033 [Peer Reviewed Journal]

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Monozygotic female twins discordant for Silver-Russell syndrome and hypomethylation of the H19-DMR.

Journal of human genetics, 2008, Vol.53(10), pp.950-955 [Peer Reviewed Journal]

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Molecular basis of complement factor I (CFI) polymorphism: one of two polymorphic suballeles responsible for CFI A is Japanese-specific.

Journal of human genetics, 2008, Vol.53(11-12), pp.1016-1021 [Peer Reviewed Journal]

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Variations in the FTO gene are associated with severe obesity in the Japanese.

Journal of human genetics, 2008, Vol.53(6), pp.546-553 [Peer Reviewed Journal]

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Gap junction beta 1 (GJB1) gene mutations in Italian patients with X-linked Charcot-Marie-Tooth disease

Journal of Human Genetics, 2008, Vol.53(6), pp.529-533 [Peer Reviewed Journal]

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by this Author/Contributor:

  1. Kamatani, Naoyuki
  2. Nakamura, Yusuke
  3. Ohashi, Jun
  4. Tokunaga, Katsushi
  5. Hirota, Tomomitsu

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