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[Publications] Minoshima,S.,Mitsuyama,S.,Ohno,S.,Kawamura,T.,and Shimizu,N.: "Eye disorder database"KMeyeDB""Human Mutation. 15. 95-98 (2000)
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[Publications] Minoshima,S.,Mitsuyama,S.,Ohno,S.,Kawamura,T.,and Shimizu,N.: "Keio Mutation Database"KMDB"for Human Disease Gene Mutations."Nucleic Acids Res. 28. 364-368 (2000)
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[Publications] The chromosome 21 mapping and sequencing consortium.Hattori,M.,36人省略,Minoshima,S.,Shimizu,N.,24人省略.: "The DNA sequence of human chromosome 21."Nature. 405. 311-319 (2000)
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[Publications] Minoshima,S.,Mitsuyama,S.,Ohtsubo,M.,Kawamura,T.,Ito,S.,Shibamoto,S.,Ito,F.and Shimizu,N.: "A New Version of the KMDB/Mutation View : A Keio Mutation Database for Human Disease Gene."Genome Informatics 2000 Universal Academic Press,Inc.,Tokyo. 224-226 (2000)
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[Publications] Minoshima,S.,Mitsuyama,S.,Ohtsubo,M.,Kawamura,T.,Ito,S.,Shibamoto,S.,Ito,F.and Shimizu,N.: "The KMDB/Mutation View : a mutation database for human disease genes.Keio Mutation Database"KMDB"for Human Disease Gene Mutations."Nucleic Acids Res. 29. 327-328 (2001)
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[Publications] Scott,H.S.,Kudoh,J.,Wattenhofer,M.,Shibuya,K.,Berry,A.,Chrast,R.,Guipponi,M.,Wang,J.,Kawasaki,K.,Asakawa,S.,Minoshima,S.,Shimizu,N. et al.: "Insertion of β-satellite repeats identifies a transmembrane protease causing both congenital and childhood onset autosomal recessive deafness."Nature Genet.. 27. 59-63 (2001)
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[Publications] Dawson,E,Chen,Y,Hunt,S,Smink,LJ,Hunt,A,Rice,K,Livingston,S,Bumpstead,S,Bruskiewich,R,Sham,P,Ganske,R,Adams,M,Kawasaki,K,Shimizu,N,Minoshima,S,Roe,B,Bentley,D,Dunham,I.: "A SNP resource for human chromosome 22: extracting dense clusters of SNPs from the genomic sequence."Genome Res.. 11. 170-8 (2001)
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[Publications] International Human Genome Sequencing Consortium: "Initial sequencing and analysis of the human genome."Nature. 409. 860-921 (2001)
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[Publications] International Human Genome Mapping Consortium: "A physical map of the human genome."Nature. 409. 934-941 (2001)
