Works matching IS 00015652 AND DT 1999 AND VI 49 AND IP 3

Results: 12

Analysis of Estrogen Receptor Dinucleotide Polymorphism by Capillary Gel Electrophoresis with a Population Genetic Study in 180 Finns.

Published in:

Human Heredity, 1999, v. 49, n. 3, p. 142, doi. 10.1159/000022862

By:

Kunnas, Tarja A.;
Holmberg-Marttila, Doris;
Karhunen, Pekka J.

Publication type:

Article

Testing for Linkage underRobust Genetic Models.

Published in:

Human Heredity, 1999, v. 49, n. 3, p. 146, doi. 10.1159/000022863

By:

Guerra, R.;
Wan, Y.;
Jia, A.;
Amos, C.I.;
Cohen, J.C.

Publication type:

Article

Detection of the Most Common G6PD Gene Mutations in Chinese Using Amplification Refractory Mutation System.

Published in:

Human Heredity, 1999, v. 49, n. 3, p. 133, doi. 10.1159/000022860

By:

Du, Chuan S.;
Ren, Xiaoqin;
Chen, Luming;
Jiang, Weiying;
He, Yongshu;
Yang, Ming

Publication type:

Article

Simple Tandem Repeat Polymorphisms in the Neuronal Nitric Oxide Synthase Gene in Different Ethnic Populations.

Published in:

Human Heredity, 1999, v. 49, n. 3, p. 139, doi. 10.1159/000022861

By:

Grasemann, Hartmut;
Drazen, Jeffrey M.;
Deykin, Aaron;
Israel, Elliot;
De Sanctis, George T.;
Pillari, Anthony;
Yandava, Chandri N.

Publication type:

Article

Localization of the Gene Responsible for Familial Benign Polycythemia to Chromosome 11q23.

Published in:

Human Heredity, 1999, v. 49, n. 3, p. 129, doi. 10.1159/000022859

By:

Vasserman, Natalia N.;
Karzakova, Luisa M.;
Tverskaya, Svetlana M.;
Saperov, Vladimir N.;
Muchukova, Olga M.;
Pavlova, Galina P.;
Efimova, Nadejda K.;
Vankina, Natalia N.;
Evgrafov, Oleg V.

Publication type:

Article

Gln → Arg 191 Polymorphism of Paraoxonase and Parkinson's Disease.

Published in:

Human Heredity, 1999, v. 49, n. 3, p. 178, doi. 10.1159/000022868

By:

Akhmedova, S.;
Anisimov, S.;
Yakimovsky, A.;
Schwartz, E.

Publication type:

Article

Familiality of Quantitative Metabolic Traits in Finnish Families with Non-Insulin-Dependent Diabetes mellitus.

Published in:

Human Heredity, 1999, v. 49, n. 3, p. 159, doi. 10.1159/000022865

By:

Watanabe, Richard M.;
Valle, Timo;
Hauser, Elizabeth R.;
Ghosh, Soumitra;
Eriksson, Johan;
Kohtamäki, Kimmo;
Ehnholm, Christian;
Tuomilehto, Jaakko;
Collins, Francis S.;
Bergman, Richard N.;
Boehnke, Michael

Publication type:

Article

Mutation Analysis in Patients with Congenital Adrenal Hyperplasia in the Spanish Population: Identification of Putative Novel Steroid 21-Hydroxylase Deficiency Alleles Associated with the Classic Form of the Disease.

Published in:

Human Heredity, 1999, v. 49, n. 3, p. 169, doi. 10.1159/000022866

By:

Lobato, M. Natividad;
Ordóñez-Sánchez, M. Luisa;
Tusié-Luna, M. Teresa;
Meseguer, Anna

Publication type:

Article

The LW<sup>b</sup> Blood Group as a Marker of Prehistoric Baltic Migrations and Admixture.

Published in:

Human Heredity, 1999, v. 49, n. 3, p. 154, doi. 10.1159/000022864

By:

Sistonen, P.;
Virtaranta-Knowles, K.;
Denisova, R.;
Kučinskas, V.;
Ambrasiene, D.;
Beckman, L.

Publication type:

Article

A Novel G to A Substitution at Nucleotide 1734 of the FBN1 Gene Predicting a C534Y Mutation Responsible for Marfan Syndrome.

Published in:

Human Heredity, 1999, v. 49, n. 3, p. 176, doi. 10.1159/000022867

By:

Kilpatrick, Michael W.;
Lembessis, Peter;
Rose, Elise;
Tsipouras, Petros

Publication type:

Article

Screening for Mutations in the Promoter and the Coding Region of the IGFBP1 and IGFBP3 Genes in Silver-Russell Syndrome Patients.

Published in:

Human Heredity, 1999, v. 49, n. 3, p. 123, doi. 10.1159/000022858

By:

Eggermann, Katja;
Wollmann, Hartmut A.;
Tomiuk, Jürgen;
Ranke, Michael B.;
Kaiser, Peter;
Eggermann, Thomas

Publication type:

Article

New AccI Polymorphism in the Follicle-Stimulating Hormone Beta-Subunit Gene andIts Prevalence in Three Southeast AsianPopulations.

Published in:

Human Heredity, 1999, v. 49, n. 3, p. 181, doi. 10.1159/000022869

By:

Liao, Wu-Xiang;
Tong, Yan;
Roy, Ashim C.;
Ng, Soon Chye

Publication type:

Article