Works matching IS 03406717 AND DT 2008 AND VI 123 AND IP 3

Results: 13

William Reardon: The Bedside Dysmorphologist.

Published in:

2008

By:

Clayton-Smith, Jill

Publication type:

Book Review

Wolf–Hirschhorn syndrome-associated chromosome changes are not mediated by olfactory receptor gene clusters nor by inversion polymorphism on 4p16.

Published in:

2008

By:

Zollino, Marcella;
Lecce, Rosetta;
Murdolo, Marina;
Orteschi, Daniela;
Marangi, Giuseppe;
Selicorni, Angelo;
Midro, Alina;
Sorge, Giovanni;
Zampino, Giuseppe;
Memo, Luigi;
Battaglia, Domenica;
Petersen, Michael;
Pandelia, Effie;
Gyftodimou, Yolanda;
Faravelli, Francesca;
Tenconi, Romano;
Garavelli, Livia;
Mazzanti, Laura;
Fischetto, Rita;
Cavalli, Pietro

Publication type:

Correction Notice

Investigating the association between K198N coding polymorphism in EDN1 and hypertension, lipoprotein levels, the metabolic syndrome and cardiovascular disease.

Published in:

Human Genetics, 2008, v. 123, n. 3, p. 307, doi. 10.1007/s00439-008-0481-0

By:

Wiltshire, Steven;
Powell, Brenda L.;
Jennens, Michelle;
McCaskie, Pamela A.;
Carter, Kim W.;
Palmer, Lyle J.;
Thompson, Peter L.;
McQuillan, Brendan M.;
Hung, Joseph;
Beilby, John P.

Publication type:

Article

Leprosy as a genetic model for susceptibility to common infectious diseases.

Published in:

Human Genetics, 2008, v. 123, n. 3, p. 227, doi. 10.1007/s00439-008-0474-z

By:

Alter, Andrea;
Alcaïs, Alexandre;
Abel, Laurent;
Schurr, Erwin

Publication type:

Article

Linkage to chromosome 2q36.1 in autosomal dominant Dandy-Walker malformation with occipital cephalocele and evidence for genetic heterogeneity.

Published in:

Human Genetics, 2008, v. 123, n. 3, p. 237, doi. 10.1007/s00439-008-0467-y

By:

Jalali, Ali;
Aldinger, Kimberly A.;
Chary, Ajit;
Mclone, David G.;
Bowman, Robin M.;
Luan Cong Le;
Jardine, Phillip;
Newbury-Ecob, Ruth;
Mallick, Andrew;
Jafari, Nadereh;
Russell, Eric J.;
Curran, John;
Nguyen, Pam;
Ouahchi, Karim;
Lee, Charles;
Dobyns, William B.;
Millen, Kathleen J.;
Pina-Neto, Joao M.;
Kessler, John A.;
Bassuk, Alexander G.

Publication type:

Article

W.A. Schultz: Molecular biology of human cancers. An advanced student’s textbook.

Published in:

2008

By:

Hodgson, Shirley

Publication type:

Book Review

Protein C -1641A/-1654C haplotype is associated with organ dysfunction and the fatal outcome of severe sepsis in Chinese Han population.

Published in:

Human Genetics, 2008, v. 123, n. 3, p. 281, doi. 10.1007/s00439-008-0476-x

By:

Qi Xing Chen;
Shui Jing Wu;
Hai Hong Wang;
Chen Lv;
Bao Li Cheng;
Guo Hao Xie;
Xiang Ming Fang

Publication type:

Article

An insertion/deletion polymorphism of the dihydrofolate reductase ( DHFR) gene is associated with serum and red blood cell folate concentrations in women.

Published in:

Human Genetics, 2008, v. 123, n. 3, p. 289, doi. 10.1007/s00439-008-0475-y

By:

Stanisiawska-Sachadyn, Anna;
Brown, Karen S.;
Mitchell, Laura E.;
Woodside, Jayne V.;
Young, Ian S.;
Scott, John M.;
Murray, Liam;
Boreham, Colin A.;
McNulty, Helene;
Strain, J. J.;
Whitehead, Alexander S.

Publication type:

Article

A genome-wide association scan for asthma in a general Australian population.

Published in:

Human Genetics, 2008, v. 123, n. 3, p. 297, doi. 10.1007/s00439-008-0477-9

By:

Hui, J.;
Oka, A.;
James, A.;
Palmer, L. J.;
Musk, A. W.;
Beilby, J.;
Inoko, H.

Publication type:

Article

Exploring gene-environment interactions in Parkinson’s disease.

Published in:

Human Genetics, 2008, v. 123, n. 3, p. 257, doi. 10.1007/s00439-008-0466-z

By:

McCulloch, Colin C.;
Kay, Denise M.;
Factor, Stewart A.;
Samii, Ali;
Nutt, John G.;
Higgins, Donald S.;
Griffith, Alida;
Roberts, John W.;
Leis, Berta C.;
Montimurro, Jennifer S.;
Zabetian, Cyrus P.;
Payami, Haydeh

Publication type:

Article

Genetic variation in IGFBP2 and IGFBP5 is associated with breast cancer in populations of African descent.

Published in:

Human Genetics, 2008, v. 123, n. 3, p. 247, doi. 10.1007/s00439-008-0468-x

By:

Garner, Chad P.;
Ding, Yuan C.;
John, Esther M.;
Ingles, Sue A.;
Olopade, Olufunmilayo I.;
Dezheng Huo;
Adebamowo, Clement;
Ogundiran, Temidayo;
Neuhausen, Susan L.

Publication type:

Article

A new locus for otosclerosis, OTSC8, maps to the pericentromeric region of chromosome 9.

Published in:

Human Genetics, 2008, v. 123, n. 3, p. 267, doi. 10.1007/s00439-008-0470-3

By:

Ali, Insaf Bel Hadj;
Thys, Melissa;
Beltaief, Najeh;
Schrauwen, Isabelle;
Hilgert, Nele;
Vanderstraeten, Kathleen;
Dieltjens, Nele;
Mnif, Emna;
Hachicha, Slah;
Besbes, Ghazi;
Arab, Saïda Ben;
Van Camp, Guy

Publication type:

Article

Haplotypic analysis of Wellcome Trust Case Control Consortium data.

Published in:

Human Genetics, 2008, v. 123, n. 3, p. 273, doi. 10.1007/s00439-008-0472-1

By:

Browning, Brian L.;
Browning, Sharon R.

Publication type:

Article