Works matching IS 03406717 AND DT 2008 AND VI 124 AND IP 4

Results: 13

A novel genetic locus for familial febrile seizures and epilepsy on chromosome 3q26.2–q26.33.

Published in:

Human Genetics, 2008, v. 124, n. 4, p. 423, doi. 10.1007/s00439-008-0566-9

By:

Xiao-Hua Dai;
Wen-Wu Chen;
Xu Wang;
Qi-Hui Zhu;
Cong Li;
Lin Li;
Mu-Gen Liu;
Wang, Qing-K.;
Jing-Yu Liu

Publication type:

Article

Association between Apolipoprotein E genotype and cerebral palsy is not confirmed in a Caucasian population.

Published in:

Human Genetics, 2008, v. 124, n. 4, p. 411, doi. 10.1007/s00439-008-0564-y

By:

McMichael, Gai L.;
Gibson, Catherine S.;
Goldwater, Paul N.;
Haan, Eric A.;
Priest, Kevin;
Dekker, Gustaaf A.;
MacLennan, Alastair H.

Publication type:

Article

Partial AZFc deletions and duplications: clinical correlates in the Italian population.

Published in:

Human Genetics, 2008, v. 124, n. 4, p. 399, doi. 10.1007/s00439-008-0561-1

By:

Giachini, Claudia;
Laface, Ilaria;
Guarducci, Elena;
Balercia, Giancarlo;
Forti, Gianni;
Krausz, Csilla

Publication type:

Article

Identifying modifier genes of monogenic disease: strategies and difficulties.

Published in:

Human Genetics, 2008, v. 124, n. 4, p. 357, doi. 10.1007/s00439-008-0560-2

By:

Génin, Emmanuelle;
Feingold, Josué;
Clerget-Darpoux, Françoise

Publication type:

Article

Osteoporosis: an evolutionary perspective.

Published in:

Human Genetics, 2008, v. 124, n. 4, p. 349, doi. 10.1007/s00439-008-0559-8

By:

Karasik, David

Publication type:

Article

Partial 5p monosomy or trisomy in 11 patients from a family with a t(5;15)(p13.3;p12) translocation.

Published in:

Human Genetics, 2008, v. 124, n. 4, p. 387, doi. 10.1007/s00439-008-0557-x

By:

Lacerda de Carvalho, Acácia Fernandes;
da Silva Bellucco, Fernanda Teixeira;
Kulikowski, Leslie Domenici;
Toralles, Maria Betênia Pereira;
Melaragno, Maria Isabel

Publication type:

Article

Association of amyloid precursor protein-binding protein, family B, member 1 with nicotine dependence in African and European American smokers.

Published in:

Human Genetics, 2008, v. 124, n. 4, p. 393, doi. 10.1007/s00439-008-0558-9

By:

Guo-Bo Chen;
Payne, Thomas J.;
Xiang-Yang Lou;
Ma, Jennie Z.;
Jun Zhu;
Li, Ming D.

Publication type:

Article

Human hereditary hearing impairment: mouse models can help to solve the puzzle.

Published in:

Human Genetics, 2008, v. 124, n. 4, p. 325, doi. 10.1007/s00439-008-0556-y

By:

Vrijens, Karen;
Van Laer, Lut;
Van Camp, Guy

Publication type:

Article

Apparent autosomal dominant keratoconus in a large Australian pedigree accounted for by digenic inheritance of two novel loci.

Published in:

Human Genetics, 2008, v. 124, n. 4, p. 379, doi. 10.1007/s00439-008-0555-z

By:

Burdon, Kathryn P.;
Coster, Douglas J.;
Charlesworth, Jac C.;
Mills, Richard A.;
Laurie, Kate J.;
Giunta, Cecilia;
Hewitt, Alex W.;
Latimer, Paul;
Craig, Jamie E.

Publication type:

Article

Elof Axel Carlson: Neither gods nor beasts. How science is changing who we think we are.

Published in:

2008

By:

Berry, Caroline

Publication type:

Book Review

The clinical characteristics of Werner syndrome: molecular and biochemical diagnosis.

Published in:

Human Genetics, 2008, v. 124, n. 4, p. 369, doi. 10.1007/s00439-008-0562-0

By:

Muftuoglu, Meltem;
Oshima, Junko;
von Kobbe, Cayetano;
Wen-Hsing Cheng;
Leistritz, Dru F.;
Bohr, Vilhelm A.

Publication type:

Article

Re-creation of the genetic composition of a founder population.

Published in:

Human Genetics, 2008, v. 124, n. 4, p. 417, doi. 10.1007/s00439-008-0565-x

By:

Klitz, William;
Maiers, Martin;
Gragert, Loren

Publication type:

Article

Association of SIRT1 gene variation with visceral obesity.

Published in:

Human Genetics, 2008, v. 124, n. 4, p. 431, doi. 10.1007/s00439-008-0567-8

By:

Peeters, Armand V.;
Beckers, Sigri;
Verrijken, An;
Mertens, Ilse;
Roevens, Peter;
Peeters, Pieter J.;
Van Hul, Wim;
Van Gaal, Luc F.

Publication type:

Article