Works matching IS 03406717 AND DT 2008 AND VI 123 AND IP 4

Results: 12

Pax6 3′ deletion results in aniridia, autism and mental retardation.

Published in:

Human Genetics, 2008, v. 123, n. 4, p. 371, doi. 10.1007/s00439-008-0484-x

By:

Davis, L.;
Meyer, K.;
Rudd, D.;
Librant, A.;
Epping, E.;
Sheffield, V.;
Wassink, T.

Publication type:

Article

Common polymorphisms of ALOX5 and ALOX5AP and risk of coronary artery disease.

Published in:

Human Genetics, 2008, v. 123, n. 4, p. 399, doi. 10.1007/s00439-008-0489-5

By:

Assimes, Themistocles;
Knowles, Joshua;
Priest, James;
Basu, Analabha;
Volcik, Kelly;
Southwick, Audrey;
Tabor, Holly;
Hartiala, Jaana;
Allayee, Hooman;
Grove, Megan;
Tabibiazar, Raymond;
Sidney, Stephen;
Fortmann, Stephen;
Go, Alan;
Hlatky, Mark;
Iribarren, Carlos;
Boerwinkle, Eric;
Myers, Richard;
Risch, Neil;
Quertermous, Thomas

Publication type:

Article

IL1B gene promoter haplotype pairs predict clinical levels of interleukin-1β and C-reactive protein.

Published in:

Human Genetics, 2008, v. 123, n. 4, p. 387, doi. 10.1007/s00439-008-0488-6

By:

Rogus, John;
Beck, James;
Offenbacher, Steven;
Huttner, Kenneth;
Iacoviello, Licia;
Latella, Maria;
de Gaetano, Monica;
Hwa-Ying Wang;
Kornman, Kenneth;
Duff, Gordon

Publication type:

Article

Genetic variants in the 8q24 locus and risk of testicular germ cell tumors.

Published in:

Human Genetics, 2008, v. 123, n. 4, p. 409, doi. 10.1007/s00439-008-0491-y

By:

Cook, Michael;
Graubard, Barry;
Quraishi, Sabah;
Yeager, Meredith;
Chanock, Stephen;
Crenshaw, Andrew;
Erickson, Ralph;
Rubertone, Mark;
Thomas, Gilles;
McGlynn, Katherine

Publication type:

Article

Chromosomal regions 22q13 and 3p25 may harbor quantitative trait loci influencing both age at menarche and bone mineral density.

Published in:

Human Genetics, 2008, v. 123, n. 4, p. 419, doi. 10.1007/s00439-008-0490-z

By:

Feng Pan;
Peng Xiao;
Yan Guo;
Yong-Jun Liu;
Hong-Yi Deng;
Recker, Robert;
Hong-Wen Deng

Publication type:

Article

Maternal cigarette smoking, metabolic gene polymorphisms, and preterm delivery: new insights on G×E interactions and pathogenic pathways.

Published in:

Human Genetics, 2008, v. 123, n. 4, p. 359, doi. 10.1007/s00439-008-0485-9

By:

Hui-Ju Tsai;
Xin Liu;
Mestan, Karen;
Yunxian Yu;
Shanchun Zhang;
Yaping Fang;
Pearson, Colleen;
Ortiz, Katherin;
Zuckerman, Barry;
Bauchner, Howard;
Cerda, Sandra;
Stubblefield, Phillip;
Xiping Xu;
Xiaobin Wang

Publication type:

Article

Comprehensive evaluation of the estrogen receptor α gene reveals further evidence for association with type 2 diabetes enriched for nephropathy in an African American population.

Published in:

Human Genetics, 2008, v. 123, n. 4, p. 333, doi. 10.1007/s00439-008-0482-z

By:

Keene, Keith;
Mychaleckyj, Josyf;
Smith, Shelly;
Leak, Tennille;
Perlegas, Peter;
Langefeld, Carl;
Herrington, David;
Freedman, Barry;
Rich, Stephen;
Bowden, Donald;
Sale, Michèle

Publication type:

Article

Evolutionary analysis of genes of two pathways involved in placental malaria infection.

Published in:

Human Genetics, 2008, v. 123, n. 4, p. 343, doi. 10.1007/s00439-008-0483-y

By:

Sikora, Martin;
Ferrer-Admetlla, Anna;
Mayor, Alfredo;
Bertranpetit, Jaume;
Casals, Ferran

Publication type:

Article

L.A. Cannizzaro and K.H. Ramesh: Cancer genomics.

Published in:

2008

By:

Barwell, Julian

Publication type:

Book Review

A new mechanism of dominance in hypophosphatasia: the mutated protein can disturb the cell localization of the wild-type protein.

Published in:

Human Genetics, 2008, v. 123, n. 4, p. 429, doi. 10.1007/s00439-008-0480-1

By:

Lia-Baldini, A.;
Brun-Heath, I.;
Carrion, C.;
Simon-Bouy, B.;
Serre, J.;
Nunes, M.;
Mornet, E.

Publication type:

Article

A haplotype at chromosome Xq27.2 confers susceptibility to prostate cancer.

Published in:

Human Genetics, 2008, v. 123, n. 4, p. 379, doi. 10.1007/s00439-008-0486-8

By:

Yaspan, Brian;
McReynolds, Kate;
Elmore, J.;
Breyer, Joan;
Bradley, Kevin;
Smith, Jeffrey

Publication type:

Article

The human gamma-glutamyltransferase gene family.

Published in:

Human Genetics, 2008, v. 123, n. 4, p. 321, doi. 10.1007/s00439-008-0487-7

By:

Heisterkamp, Nora;
Groffen, John;
Warburton, David;
Sneddon, Tam

Publication type:

Article