Works matching IS 03406717 AND DT 2007 AND VI 122 AND IP 2

Results: 10

The COL1A1 gene and high myopia susceptibility in Japanese.

Published in:

Human Genetics, 2007, v. 122, n. 2, p. 151, doi. 10.1007/s00439-007-0388-1

By:

Inamori, Yumiko;
Ota, Masao;
Inoko, Hidetoshi;
Okada, Eiichi;
Nishizaki, Ritsuko;
Shiota, Tomoko;
Mok, Jeewon;
Oka, Akira;
Ohno, Shigeaki;
Mizuki, Nobuhisa

Publication type:

Article

Evaluation of the SNP tagging approach in an independent population sample—array-based SNP discovery in Sami.

Published in:

Human Genetics, 2007, v. 122, n. 2, p. 141, doi. 10.1007/s00439-007-0379-2

By:

Johansson, Åsa;
Vavruch-Nilsson, Veronika;
Cox, David;
Frazer, Kelly;
Gyllensten, Ulf

Publication type:

Article

High-density single nucleotide polymorphism array analysis in patients with germline deletions of 22q11.2 and malignant rhabdoid tumor.

Published in:

Human Genetics, 2007, v. 122, n. 2, p. 117, doi. 10.1007/s00439-007-0386-3

By:

Jackson, Eric;
Shaikh, Tamim;
Gururangan, Sridharan;
Jones, Marilyn;
Malkin, David;
Nikkel, Sarah;
Zuppan, Craig;
Wainwright, Luanne;
Zhang, Fan;
Biegel, Jaclyn

Publication type:

Article

Common genetic variation in eight genes of the GH/ IGF1 axis does not contribute to adult height variation.

Published in:

Human Genetics, 2007, v. 122, n. 2, p. 129, doi. 10.1007/s00439-007-0385-4

By:

Lettre, Guillaume;
Butler, Johannah;
Ardlie, Kristin;
Hirschhorn, Joel

Publication type:

Article

Imprinting detection by extending a regression-based QTL analysis method.

Published in:

Human Genetics, 2007, v. 122, n. 2, p. 159, doi. 10.1007/s00439-007-0387-2

By:

Gorlova, Olga;
Lei Lei;
Zhu, Dakai;
Shih-Feng Weng;
Shete, Sanjay;
Yiqun Zhang;
Wei-Dong Li;
Arlen Price, R.;
Amos, Christopher

Publication type:

Article

NR2A and NR2B receptor gene variations modify age at onset in Huntington disease in a sex-specific manner.

Published in:

Human Genetics, 2007, v. 122, n. 2, p. 175, doi. 10.1007/s00439-007-0393-4

By:

Arning, Larissa;
Saft, Carsten;
Wieczorek, Stefan;
Andrich, Jürgen;
Kraus, Peter;
Epplen, Jörg

Publication type:

Article

A new locus for split hand/foot malformation with long bone deficiency (SHFLD) at 2q14.2 identified from a chromosome translocation.

Published in:

Human Genetics, 2007, v. 122, n. 2, p. 191, doi. 10.1007/s00439-007-0390-7

By:

Babbs, Christian;
Heller, Raoul;
Everman, David;
Crocker, Mark;
Twigg, Stephen;
Schwartz, Charles;
Giele, Henk;
Wilkie, Andrew

Publication type:

Article

Protein C promoter polymorphisms associate with sepsis in children with systemic meningococcemia.

Published in:

Human Genetics, 2007, v. 122, n. 2, p. 183, doi. 10.1007/s00439-007-0392-5

By:

Binder, Alexander;
Endler, Georg;
Rieger, Sandra;
Geishofer, Gotho;
Resch, Bernhard;
Mannhalter, Christine;
Zenz, Werner

Publication type:

Article

Sequence variants in the genes for the interleukin-23 receptor ( IL23R) and its ligand ( IL12B) confer protection against psoriasis.

Published in:

Human Genetics, 2007, v. 122, n. 2, p. 201, doi. 10.1007/s00439-007-0397-0

By:

Capon, Francesca;
Meglio, Paola;
Szaub, Joanna;
Prescott, Natalie;
Dunster, Christina;
Baumber, Laura;
Timms, Kirsten;
Gutin, Alexander;
Abkevic, Victor;
Burden, A.;
Lanchbury, Jerry;
Barker, Jonathan;
Trembath, Richard;
Nestle, Frank

Publication type:

Article

Human Gene Mutations.

Published in:: Human Genetics, 2007, v. 122, n. 2, p. 207, doi. 10.1007/s00439-007-0398-z
Publication type:: Article