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Integrated analysis of cancer-related pathways affected by genetic and epigenetic alterations in gastric cancer

Gastric Cancer, 2015, Vol.18(1), pp.65-76 [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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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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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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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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Analysis of GADD45A sequence variations in French Canadian families with high risk of breast cancer.

Journal of human genetics, 2008, Vol.53(6), pp.490-498 [Peer Reviewed Journal]

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PTPN11, SOS1, KRAS, and RAF1 gene analysis, and genotype-phenotype correlation in Korean patients with Noonan syndrome.

Journal of human genetics, 2008, Vol.53(11-12), pp.999-1006 [Peer Reviewed Journal]

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NEFL Pro22Arg mutation in Charcot-Marie-Tooth disease type 1.

Journal of human genetics, 2008, Vol.53(10), pp.936-940 [Peer Reviewed Journal]

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Screening of BCS1L mutations in severe neonatal disorders suspicious for mitochondrial cause.

Journal of human genetics, 2008, Vol.53(6), pp.554-558 [Peer Reviewed Journal]

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by this Author/Contributor:

  1. Simard, Jacques
  2. Labrie, Yvan
  3. Durocher, Francine
  4. Izuma, Shinji
  5. Kushima, Ryoji

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