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[文献書誌] Makino M.: "Mitochondrial DNA mutations in Leigh Syndrome and their phylogenetic implications."Journal of Human Genetics. 45. 69-75 (2000)
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[文献書誌] Fucharoen G.: "Mitochondrial DNA polymorphisms in Thailand/"Journal of Human Genetics. 46. 115-125 (2001)
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[文献書誌] Qian Y.P.: "Mitochondrial DNA polymorphisms in Yunnan nationalities in China."Journal of Human Genetics. 46(In press). (2001)
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[文献書誌] 寶来聰: "ミトコンドリアゲノムからみた日本人"「現代医療」特集:ゲノム医学の現在と未来. 32(1). 285-289 (2000)
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[文献書誌] 寶来聰: "DNAから読む縄文-遺伝子から探る縄文人の系譜"白い国の詩. 523. 18-21 (2000)
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[文献書誌] 寶来聰: "ミトコンドリアDNAからみた人類の起源と拡散"「蛋白質拡散酵素」特集:人類の起源と進化をDNAレベルで探る. 45(16). 2579-2587 (2000)
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[文献書誌] Yuasa I.: "[CDG syndrome]."Ryoikibetsu Shokogun Shirizu.. (29Pt4). 493-495 (2000)
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[文献書誌] Nakamura H.: "The rearrangement of the human alpha (1)-acid Glycoprotein/Orosomucoid gene : evidence for tandemly triplicated genes consisting of two AGP1 and one Agp2"Biochem Biophys Res Commum.. 276(2). 779-784 (2000)
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[文献書誌] Watanabe G.: "a hypervariable tetranucleotide STR polymorphism on the X chromosome"Int J Legal Med.. 113(4). 249-250 (2000)
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[文献書誌] Watanabe G.: "Improved haplotype analysis of human myelin basic protein short tandem repeat loci."Hum Biol.. 72(3). 489-498 (2000)
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[文献書誌] Hoshiya S.: "Serological diagnosis of Helicobacter pylori infection."Nippon Rinsho. 59(2). 259-264 (2001)
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[文献書誌] Ohashi J.: "Computer simulation analysis suggests weak balancing selection operative at the MICA locus"Hereditas. 133(1). 25-28 (2000)
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[文献書誌] Takahata N.: "Testing Multiregionality of Modern Human Origins."Mol Biol Evol.. 18. 172-183 (2001)
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[文献書誌] Figueroa F.: "Mhc class II B gene evolution in East African cichlid fishes."Immunogenetics.. 51(7). 556-575 (2000)
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[文献書誌] Nagl S.: "The origin and age of haplochromine fishes in Lake Victoria, east Africa"Proc R Soc Lond B Biol Sci.. 267(1447). 1049-1061 (2000)
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[文献書誌] Takahata N.: "Helium flux from a sedimentary basin."Appl Radiat Isot.. 52(4). 985-992 (2000)
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[文献書誌] Satta Y.: "DNA archives and our nearest relative : the trichotomy problem revisited."Mol Phylogenet Evol.. 14(2). 259-275 (2000)
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[文献書誌] Nakamura H.: "Molecular analysis of the human orosomucoid gene ORM1^*QOkoln responsible for incompatibility in a German paternity case."Int J Legal Med.. 114(1-2). 114-117 (2000)