Works matching IS 00034800 AND DT 2010 AND VI 74 AND IP 4

Results: 12

Analysis of RET, ZEB2, EDN3 and GDNF Genomic Rearrangements in Central Congenital Hyperventilation Syndrome Patients by Multiplex Ligation-dependent Probe Amplification.

Published in:

Annals of Human Genetics, 2010, v. 74, n. 4, p. 369, doi. 10.1111/j.1469-1809.2010.00577.x

By:

Serra, Alexandre;
Görgens, Heike;
Alhadad, Karin;
Fitze, Guido;
Schackert, Hans K.

Publication type:

Article

Association of polymorphisms in the BDNF, DRD1 and DRD3 genes with tobacco smoking in schizophrenia.

Published in:

Annals of Human Genetics, 2010, v. 74, n. 4, p. 291, doi. 10.1111/j.1469-1809.2010.00578.x

By:

Novak, Gabriela;
LeBlanc, Martha;
Zai, Clement;
Shaikh, Sajid;
Renou, Julien;
DeLuca, Vincenzo;
Bulgin, Natalie;
Kennedy, James L.;
Le Foll, Bernard

Publication type:

Article

The Impact of Incomplete Linkage Disequilibrium and Genetic Model Choice on the Analysis and Interpretation of Genome-wide Association Studies.

Published in:

Annals of Human Genetics, 2010, v. 74, n. 4, p. 375, doi. 10.1111/j.1469-1809.2010.00579.x

By:

Iles, Mark M.

Publication type:

Article

A Validation Study of Type 2 Diabetes-related Variants of the TCF7L2, HHEX, KCNJ11, and ADIPOQ Genes in one Endogamous Ethnic Group of North India.

Published in:

Annals of Human Genetics, 2010, v. 74, n. 4, p. 361, doi. 10.1111/j.1469-1809.2010.00580.x

By:

Gupta, Vipin;
Khadgawat, Rajesh;
NG, Hon Keung Tony;
Kumar, Satish;
Aggarwal, Ajay;
Rao, Vadlamudi Raghavendra;
Sachdeva, M. P.

Publication type:

Article

Spectrum and Frequency of SLC26A4 Mutations Among Czech Patients with Early Hearing Loss with and without Enlarged Vestibular Aqueduct (EVA).

Published in:

Annals of Human Genetics, 2010, v. 74, n. 4, p. 299, doi. 10.1111/j.1469-1809.2010.00581.x

By:

Pourová, Radka;
Janoušek, Petr;
Jurovčík, Michal;
Dvořáková, Marcela;
Malíková, Marcela;
Rašková, Dagmar;
Bendová, Olga;
Leonardi, Emanuela;
Murgia, Alessandra;
Kabelka, Zdenek;
Astl, Jaromír;
Seeman, Pavel

Publication type:

Article

Genetic Diversity of the Fragile X Syndrome Gene ( FMR1) in a Large Sub-Saharan West African Population.

Published in:

Annals of Human Genetics, 2010, v. 74, n. 4, p. 316, doi. 10.1111/j.1469-1809.2010.00582.x

By:

Peprah, Emmanuel K.;
Allen, Emily G.;
Williams, Scott M.;
Woodard, Laresa M.;
Sherman, Stephanie L.

Publication type:

Article

Erratum.

Published in:: 2010
Publication type:: Correction Notice

Association of SLC6A12 variants with aspirin-intolerant asthma in a Korean population.

Published in:

Annals of Human Genetics, 2010, v. 74, n. 4, p. 326, doi. 10.1111/j.1469-1809.2010.00584.x

By:

Pasaje, Charisse Flerida A.;
Jeong-Hyun Kim;
Byung-Lae Park;
Hyun Sub Cheong;
Ji-Yong Chun;
Tae-Joon Park;
Jin-Sol Lee;
Yongha Kim;
Joon Seol Bae;
Jong Sook Park;
Sang-Hyuk Yoon;
Soo-Taek Uh;
Jae-Sung Choi;
Yong-Hoon Kim;
Mi-Kyeong Kim;
Choi, Inseon S.;
Sang Heon Cho;
Byoung Whui Choi;
Choon-Sik Park;
Hyoung Doo Shin

Publication type:

Article

Elucidation of CYP2D6 Genetic Diversity in a Unique African Population: Implications for the Future Application of Pharmacogenetics in the Xhosa Population.

Published in:

Annals of Human Genetics, 2010, v. 74, n. 4, p. 340, doi. 10.1111/j.1469-1809.2010.00585.x

By:

Wright, Galen E. B.;
Niehaus, Dana J. H.;
Drögemöller, Britt I.;
Koen, Liezl;
Gaedigk, Andrea;
Warnich, Louise

Publication type:

Article

Influence of the leptin G-2548A polymorphism on leptin levels and anthropometric measurements in healthy Spanish adolescents.

Published in:

Annals of Human Genetics, 2010, v. 74, n. 4, p. 335, doi. 10.1111/j.1469-1809.2010.00586.x

By:

Riestra, Pia;
Garcia-Anguita, Alicia;
Viturro, Enrique;
Schoppen, Stefanie;
de Oya, Manuel;
Garcés, Carmen

Publication type:

Article

Influence of population stratification on population-based marker-disease association analysis.

Published in:

Annals of Human Genetics, 2010, v. 74, n. 4, p. 351, doi. 10.1111/j.1469-1809.2010.00588.x

By:

Tengfei Li;
Zhaohai Li;
Zhiliang Ying;
Hong Zhang

Publication type:

Article

Univariate and Bivariate Linkage Analysis Identifies Pleiotropic Loci Underlying Lipid Levels and Type 2 Diabetes Risk.

Published in:

Annals of Human Genetics, 2010, v. 74, n. 4, p. 308, doi. 10.1111/j.1469-1809.2010.00589.x

By:

Hasstedt, Sandra J.;
Hanis, Craig L.;
Elbein, Steven C.

Publication type:

Article