Works matching IS 03406717 AND DT 2008 AND VI 124 AND IP 2

Results: 11

A new susceptibility locus for hypospadias on chromosome 7q32.2-q36.1.

Published in:

Human Genetics, 2008, v. 124, n. 2, p. 155, doi. 10.1007/s00439-008-0533-5

By:

Thai, Hanh T. T.;
Söderhäll, Cilla;
Lagerstedt, Kristina;
Davood Omrani, Mir;
Fris&a#x00E9;n, Louise;
Lundin, Johanna;
Kockum, Ingrid;
Nordenskjöld, Agneta

Publication type:

Article

Exploration of the utility of ancestry informative markers for genetic association studies of African Americans with type 2 diabetes and end stage renal disease.

Published in:

Human Genetics, 2008, v. 124, n. 2, p. 147, doi. 10.1007/s00439-008-0532-6

By:

Keene, Keith L.;
Mychaleckyj, Josyf C.;
Leak, Tennille S.;
Smith, Shelly G.;
Perlegas, Peter S.;
Divers, Jasmin;
Langefeld, Carl D.;
Freedman, Barry I.;
Bowden, Donald W.;
Sale, Michèle M.

Publication type:

Article

Evolutionary dynamics of the human ABO gene.

Published in:

Human Genetics, 2008, v. 124, n. 2, p. 123, doi. 10.1007/s00439-008-0530-8

By:

Calafell, Francesc;
Roubine3, Francis;
Ramírez-Soriano, Anna;
Saitou, Naruya;
Bertranpetit, Jaume;
Blancher, Antoine

Publication type:

Article

Somatic mosaicism for a PDHA1 mutation in a female with pyruvate dehydrogenase deficiency.

Published in:

Human Genetics, 2008, v. 124, n. 2, p. 187, doi. 10.1007/s00439-008-0538-0

By:

Ridout, Cheryl K.;
Brown, Ruth M.;
Walter, John H.;
Brown, Garry K.

Publication type:

Article

Comprehensive resequence analysis of a 136 kb region of human chromosome 8q24 associated with prostate and colon cancers.

Published in:

Human Genetics, 2008, v. 124, n. 2, p. 161, doi. 10.1007/s00439-008-0535-3

By:

Yeager, Meredith;
Nianqing Xiao;
Hayes, Richard B.;
Bouffard, Pascal;
Desany, Brian;
Burdett, Laura;
Orr, Nick;
Matthews, Casey;
Liqun Qi;
Crenshaw, Andrew;
Markovic, Zdenek;
Fredrikson, Karin M.;
Jacobs, Kevin B.;
Amundadottir, Laufey;
Jarvie, Thomas P.;
Hunter, David J.;
Hoover, Robert;
Thomas, Gilles;
Harkins, Timothy T.;
Chanock, Stephen J.

Publication type:

Article

Exploration of the utility of ancestry informative markers for genetic association studies of African Americans with type 2 diabetes and end stage renal disease.

Published in:

2008

By:

Keene, Keith L.;
Mychaleckyj, Josyf C.;
Leak, Tennille S.;
Smith, Shelly G.;
Perlegas, Peter S.;
Divers, Jasmin;
Langefeld, Carl D.;
Freedman, Barry I.;
Bowden, Donald W.;
Sale, Michèle M.

Publication type:

Correction Notice

Constitutional mismatch repair-deficiency syndrome: have we so far seen only the tip of an iceberg?

Published in:

Human Genetics, 2008, v. 124, n. 2, p. 105, doi. 10.1007/s00439-008-0542-4

By:

Wimmer, Katharina;
Etzler, Julia

Publication type:

Article

Genetic studies of African populations: an overview on disease susceptibility and response to vaccines and therapeutics.

Published in:

2008

By:

Sirugo, Giorgio;
Hennig, Branwen J.;
Adeyemo, Adebowale A.;
Matimba, Alice;
Newport, Melanie J.;
Ibrahim, Muntaser E.;
Ryckman, Kelli K.;
Tacconelli, Alessandra;
Mariani-Costantini, Renato;
Novelli, Giuseppe;
Soodyall, Himla;
Rotimi, Charles N.;
Ramesar, Raj S.;
Tishkoff, Sarah A.;
Williams, Scott M.

Publication type:

Correction Notice

Polymorphisms of the tumor necrosis factor-alpha receptor 2 gene are associated with obesity phenotypes among 405 Caucasian nuclear families.

Published in:

Human Genetics, 2008, v. 124, n. 2, p. 171, doi. 10.1007/s00439-008-0536-2

By:

Lan-Juan Zhao;
Dong-Hai Xiong;
Feng Pan;
Xiao-Gang Liu;
Recker, Robert R.;
Hong-Wen Deng

Publication type:

Article

A replication study confirmed the EDAR gene to be a major contributor to population differentiation regarding head hair thickness in Asia.

Published in:

Human Genetics, 2008, v. 124, n. 2, p. 179, doi. 10.1007/s00439-008-0537-1

By:

Fujimoto, Akihiro;
Ohashi, Jun;
Nishida, Nao;
Miyagawa, Taku;
Morishita, Yasuyuki;
Tsunoda, Tatsuhiko;
Kimura, Ryosuke;
Tokunaga, Katsushi

Publication type:

Article

Reduced folate carrier 80A→G polymorphism, plasma folate, and risk of placental abruption.

Published in:

Human Genetics, 2008, v. 124, n. 2, p. 137, doi. 10.1007/s00439-008-0531-7

By:

Ananth, Cande V.;
Peltier, Morgan R.;
Moore, Dirk F.;
Kinzler, Wendy L.;
Leclerc, Daniel;
Rozen, Rima R.

Publication type:

Article