Works matching IS 00015652 AND DT 2001 AND VI 51 AND IP 1/2

Results: 16

Epidemiology and Factor Analysis of Obesity, Type II Diabetes, Hypertension, and Dyslipidemia (Syndrome X) on the Island of Kosrae, Federated States of Micronesia.

Published in:

Human Heredity, 2001, v. 51, n. 1/2, p. 8, doi. 10.1159/000022953

By:

Shmulewitz, Dvora;
Auerbach, Steven B.;
Lehner, Thomas;
Blundell, Maude L.;
Winick, Jeffrey D.;
Youngman, Linda D.;
Skilling, Vita;
Heath, Simon C.;
Ott, Jürg;
Stoffel, Markus;
Breslow, Jan L.;
Friedman, Jeffrey M.

Publication type:

Article

C677T Methylenetetrahydrofolate Reductase Polymorphism Is Not a Risk Factor for Pre-Eclampsia/Eclampsia among Australian Women.

Published in:

Human Heredity, 2001, v. 51, n. 1/2, p. 20, doi. 10.1159/000022954

By:

Kaiser, Thomas;
Brennecke, Shaun P.;
Moses, Eric K.

Publication type:

Article

Ascertainment and Anticipation in Family Studies.

Published in:

Human Heredity, 2001, v. 51, n. 1/2, p. 23, doi. 10.1159/000022955

By:

Hoh, Josephine;
Heitjan, Daniel F.;
Mérette, Chantal;
Ott, Jürg

Publication type:

Article

Consanguinity in South America: Demographic Aspects.

Published in:

Human Heredity, 2001, v. 51, n. 1/2, p. 27, doi. 10.1159/000022956

By:

Liascovich, Rosa;
Rittler, Mónica;
Castilla, Eduardo E.

Publication type:

Article

Risk Ratios for Obesity in Families of Obese African-American and Caucasian Women.

Published in:

Human Heredity, 2001, v. 51, n. 1/2, p. 35, doi. 10.1159/000022957

By:

Price, R. Arlen;
Lee, Joseph H.

Publication type:

Article

The C677T Mutation of the Methylenetetrahydrofolate Reductase Gene Is Not Associated with the Risk of Coronary Artery Disease or Venous Thrombosis among Chinese in Taiwan.

Published in:

Human Heredity, 2001, v. 51, n. 1/2, p. 41, doi. 10.1159/000022958

By:

Hsu, Lung-An;
Ko, Yu-Lin;
Wang, Shu-Mei;
Chang, Chi-Jen;
Hsu, Tsu-Shiu;
Chiang, Cheng-Wen;
Lee, Ying-Shiung

Publication type:

Article

Association Tests for Traits with Variable Age at Onset.

Published in:

Human Heredity, 2001, v. 51, n. 1/2, p. 46, doi. 10.1159/000022959

By:

Mokliatchouk, Oksana;
Blacker, Deborah;
Rabinowitz, Daniel

Publication type:

Article

β-Globin Gene Haplotype Characteristics of Colombian Amerinds in South America.

Published in:

Human Heredity, 2001, v. 51, n. 1/2, p. 54, doi. 10.1159/000022960

By:

Shimizu, Koji;
Hashimoto, Toyoko;
Harihara, Shinji;
Tajima, Kazuo;
Sonoda, Shunro;
Zaninovic, Vladimir

Publication type:

Article

A Robust Identity-by-Descent Procedure Using Affected Sib Pairs: Multipoint Mapping for Complex Diseases.

Published in:

Human Heredity, 2001, v. 51, n. 1/2, p. 64, doi. 10.1159/000022961

By:

Liang, Kung-Yee;
Chiu, Yen-Feng;
Beaty, Terri H.

Publication type:

Article

The Split of the Arara Population: Comparison of Genetic Drift and Founder Effect.

Published in:

Human Heredity, 2001, v. 51, n. 1/2, p. 79, doi. 10.1159/000022962

By:

Ribeiro-dos-Santos, Ândrea K.C.;
Guerreiro, João Farias;
Santos, Sidney E.B.;
Zago, Marco Antonio

Publication type:

Article

Haplotype Evolution and Linkage Disequilibrium: A Simulation Study.

Published in:

Human Heredity, 2001, v. 51, n. 1/2, p. 85, doi. 10.1159/000022963

By:

Calafell, Francesc;
Grigorenko, Elena L.;
Chikanian, Alexei A.;
Kidd, Kenneth K.

Publication type:

Article

Genetic Diversity in an Andean Population from Peru and Regional Migration Patterns of Amerindians in South America: Data from Y Chromosome and Mitochondrial DNA.

Published in:

Human Heredity, 2001, v. 51, n. 1/2, p. 97, doi. 10.1159/000022964

By:

Rodriguez-Delfin, Luis A.;
Rubin-de-Celis, Verónica E.;
Zago, Marco A.

Publication type:

Article

Genetic Linkage Analysis of Prostate Cancer Families to Xq27-28.

Published in:

Human Heredity, 2001, v. 51, n. 1/2, p. 107, doi. 10.1159/000022965

By:

Peters, Mette A.;
Jarvik, Gail P.;
Janer, Marta;
Chakrabarti, Lisa;
Kolb, Suzanne;
Goode, Ellen L.;
Gibbs, Mark;
DuBois, Charles C.;
Schuster, Eugene F.;
Hood, Leroy;
Ostrander, Elaine A.;
Stanford, Janet L.

Publication type:

Article

Identification of mtDNA Mutation in a Pedigree with Gestational Diabetes, Deafness, Wolff-Parkinson-White Syndrome and Placenta accreta.

Published in:

Human Heredity, 2001, v. 51, n. 1/2, p. 114, doi. 10.1159/000022950

By:

Aggarwal, P.;
Gill-Randall, R.;
Wheatley, T.;
Buchalter, M.B.;
Metcalfe, J.;
Alcolado, J.C.

Publication type:

Article

Association between Minihaplotypes and Mutations at the PAH Locus in Polish Hyperphenylalaninemic Patients.

Published in:

Human Heredity, 2001, v. 51, n. 1/2, p. 117, doi. 10.1159/000022951

By:

Żekanowski, Cezary;
Jurkowska, Monika;
Bal, Jerzy

Publication type:

Article

The API2/MALT1 Fusion Product May Lead to Germinal Center B Cell Lymphomas by Suppression of Apoptosis.

Published in:

Human Heredity, 2001, v. 51, n. 1/2, p. 1, doi. 10.1159/000022952

By:

Stoffel, Archontoula;
Le Beau, Michelle M.

Publication type:

Article