Works matching IS 14345161 AND DT 2004 AND VI 49 AND IP 9

Results: 8

Comparison between various strategies for the disease-gene mapping using linkage disequilibrium analyses: studies on adenine phosphoribosyltransferase deficiency used as an example.
Published in:
Journal of Human Genetics, 2004, v. 49, n. 9, p. 463, doi. 10.1007/s10038-004-0175-y
By:
- Kuno, Shin-ichi;
- Taniguchi, Atsuo;
- Saito, Akira;
- Tsuchida-Otsuka, Sanae;
- Kamatani, Naoyuki
Publication type:
Article
Association of paraoxonase 1 gene polymorphisms with risk of Parkinson’s disease: a meta-analysis.
Published in:
Journal of Human Genetics, 2004, v. 49, n. 9, p. 474, doi. 10.1007/s10038-004-0176-x
By:
- Zintzaras, Elias;
- Hadjigeorgiou, Georgios M.
Publication type:
Article
Genetic background of people in the Dominican Republic with or without obese type 2 diabetes revealed by mitochondrial DNA polymorphism.
Published in:
Journal of Human Genetics, 2004, v. 49, n. 9, p. 495, doi. 10.1007/s10038-004-0179-7
By:
- Tajima, Atsushi;
- Hamaguchi, Kazuyuki;
- Terao, Hideo;
- Oribe, Ayako;
- Perrotta, Victor M.;
- Baez, Carlos Amoros;
- Arias, Jose R.;
- Yoshimatsu, Hironobu;
- Sakata, Toshiie;
- Horai, Satoshi
Publication type:
Article
Association between the PPARa-L162V polymorphism and components of the metabolic syndrome.
Published in:
Journal of Human Genetics, 2004, v. 49, n. 9, p. 482, doi. 10.1007/s10038-004-0177-9
By:
- Robitaille, Julie;
- Brouillette, Charles;
- Houde, Alain;
- Lemieux, Simone;
- Pérusse, Louis;
- Tchernof, André;
- Gaudet, Daniel;
- Vohl, Marie-Claude
Publication type:
Article
Characterization of a new PEPD allele causing prolidase deficiency in two unrelated patients: natural-occurrent mutations as a tool to investigate structure-function relationship.
Published in:
Journal of Human Genetics, 2004, v. 49, n. 9, p. 500, doi. 10.1007/s10038-004-0180-1
By:
- Lupi, Anna;
- De Riso, Antonio;
- Della Torre, Sara;
- Rossi, Antonio;
- Campari, Elena;
- Vilarinho, Laura;
- Cetta, Giuseppe;
- Forlino, Antonella
Publication type:
Article
Identification of 108 SNPs inTSC,WNK1, andWNK4and their association with hypertension in a Japanese general population.
Published in:
Journal of Human Genetics, 2004, v. 49, n. 9, p. 507, doi. 10.1007/s10038-004-0181-0
By:
- Kokubo, Yoshihiro;
- Kamide, Kei;
- Inamoto, Nozomu;
- Tanaka, Chihiro;
- Banno, Mariko;
- Takiuchi, Shin;
- Kawano, Yuhei;
- Tomoike, Hitonobu;
- Miyata, Toshiyuki
Publication type:
Article
Identification of a common mutation in mucopolysaccharidosis IVA: correlation among genotype, phenotype, and keratan sulfate.
Published in:
Journal of Human Genetics, 2004, v. 49, n. 9, p. 490, doi. 10.1007/s10038-004-0178-8
By:
- Tomatsu, Shunji;
- Dieter, Tatiana;
- Schwartz, Ida V.;
- Sarmient, Piedad;
- Giugliani, Roberto;
- Barrera, Luis A.;
- Guelbert, Norberto;
- Kremer, Raquel;
- Repetto, Gabriela M.;
- Gutierrez, Monica A.;
- Nishioka, Tatsuo;
- Peña Serrato, Olga;
- Montaño, Adriana Maria;
- Yamaguchi, Seiji;
- Noguchi, Akihiko
Publication type:
Article
High throughput multiple combination extraction from large scale polymorphism data by exact tree method.
Published in:
Journal of Human Genetics, 2004, v. 49, n. 9, p. 455, doi. 10.1007/s10038-004-0174-z
By:
- Miyaki, Koichi;
- Omae, Kazuyuki;
- Murata, Mitsuru;
- Tanahashi, Norio;
- Saito, Ikuo;
- Watanabe, Kiyoaki
Publication type:
Article