Works matching IS 03406717 AND DT 2008 AND VI 122 AND IP 6

Results: 12

Discovering DNA: Friedrich Miescher and the early years of nucleic acid research.

Published in:

Human Genetics, 2008, v. 122, n. 6, p. 565, doi. 10.1007/s00439-007-0433-0

By:

Dahm, Ralf

Publication type:

Article

Localization of a novel gene for congenital nonsyndromic simple microphthalmia to chromosome 2q11-14.

Published in:

Human Genetics, 2008, v. 122, n. 6, p. 589, doi. 10.1007/s00439-007-0435-y

By:

Hui Li;
Jia-Xin Wang;
Cheng-Ye Wang;
Ping Yu;
Qiang Zhou;
Yong-Gang Chen;
Lu-Hang Zhao;
Ya-Ping Zhang

Publication type:

Article

Parental transmission of HLA-DRB1*15 in multiple sclerosis.

Published in:

Human Genetics, 2008, v. 122, n. 6, p. 661, doi. 10.1007/s00439-007-0442-z

By:

Ramagopalan, Sreeram V.;
Herrera, Blanca M.;
Bell, Jordana T.;
Dyment, David A.;
DeLuca, Gabriele C.;
Lincoln, Matthew R.;
Orton, Sarah M.;
Chao, Michael J.;
Sadovnick, A. Dessa;
Ebers, George C.

Publication type:

Article

A genome-wide approach to identifying novel-imprinted genes.

Published in:

Human Genetics, 2008, v. 122, n. 6, p. 625, doi. 10.1007/s00439-007-0440-1

By:

Pollard, Katherine;
Serre, David;
Xu Wang;
Heng Tao;
Grundberg, Elin;
Hudson, Thomas;
Clark, Andrew;
Frazer, Kelly

Publication type:

Article

Eberhard Passarge: Color atlas of genetics.

Published in:

2008

By:

Dennis, Nicholas Robert

Publication type:

Book Review

A new syndrome with noncompaction cardiomyopathy, bradycardia, pulmonary stenosis, atrial septal defect and heterotaxy with suggestive linkage to chromosome 6p.

Published in:

Human Genetics, 2008, v. 122, n. 6, p. 595, doi. 10.1007/s00439-007-0436-x

By:

Wessels, Marja W.;
Graaf, Bianca M.;
Cohen-Overbeek, Titia E.;
Spitaels, Silja E.;
Groot-de Laat, Lotte E.;
Ten Cate, Folkert J.;
Frohn-Mulder, Ingrid F. M.;
de Krijger, Ronald;
Bartelings, Margot M.;
Essed, Nienke;
Wladimiroff, Jury W.;
Niermeijer, Martinus F.;
Heutink, Peter;
Oostra, Ben A.;
Dooijes, Dennis;
Bertoli-Avella, Aida M.;
Willems, Patrick J.

Publication type:

Article

CFTR mutations and reproductive outcomes in a population isolate.

Published in:

Human Genetics, 2008, v. 122, n. 6, p. 583, doi. 10.1007/s00439-007-0432-1

By:

Romero, Irene Gallego;
Ober, Carole

Publication type:

Article

Evidence for linkage of a new region (11p14) to eczema and allergic diseases.

Published in:

Human Genetics, 2008, v. 122, n. 6, p. 605, doi. 10.1007/s00439-007-0439-7

By:

Guilloud-Bataille, Michel;
Bouzigon, Emmanuelle;
Annesi-Maesano, Isabella;
Bousquet, Jean;
Charpin, Denis;
Gormand, Frédéric;
Hochez, Joëlle;
Just, Jocelyne;
Lemainque, Arnaud;
Moual, Nicole;
Matran, Régis;
Neukirch, Françoise;
Oryszczyn, Marie-Pierre;
Paty, Evelyne;
Pin, Isabelle;
Vervloet, Daniel;
Kauffmann, Francine;
Lathrop, Mark;
Demenais, Florence;
Dizier, Marie-Hélène

Publication type:

Article

Positive association between OLIG2 and schizophrenia in the Chinese Han population.

Published in:

Human Genetics, 2008, v. 122, n. 6, p. 659, doi. 10.1007/s00439-007-0434-z

By:

Ke Huang;
Wei Tang;
Ruqi Tang;
Zhao Xu;
Zhangdong He;
Zhiqiang Li;
Yifeng Xu;
Xingwang Li;
Guang He;
Guoying Feng;
Lin He;
YongYong Shi

Publication type:

Article

Moderate reduction of Norrin signaling activity associated with the causative missense mutations identified in patients with familial exudative vitreoretinopathy.

Published in:

Human Genetics, 2008, v. 122, n. 6, p. 615, doi. 10.1007/s00439-007-0438-8

By:

Minghui Qin;
Kondo, Hiroyuki;
Tahira, Tomoko;
Hayashi, Kenshi

Publication type:

Article

Induction of full-length survival motor neuron by polyphenol botanical compounds.

Published in:

Human Genetics, 2008, v. 122, n. 6, p. 635, doi. 10.1007/s00439-007-0441-0

By:

Sakla, Mary S.;
Lorson, Christian L.

Publication type:

Article

Functional characterization of the human TPH2 5′ regulatory region: untranslated region and polymorphisms modulate gene expression in vitro.

Published in:

Human Genetics, 2008, v. 122, n. 6, p. 645, doi. 10.1007/s00439-007-0443-y

By:

Guo-Lin Chen;
Vallender, Eric J.;
Miller, Gregory M.

Publication type:

Article