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

Results: 13

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
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
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
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
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
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
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
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