Works matching IS 10184813 AND DT 2003 AND VI 11 AND IP 3

Results: 11

Reduced folate carrier polymorphism (80A?G) and neural tube defects.

Published in:

European Journal of Human Genetics, 2003, v. 11, n. 3, p. 245, doi. 10.1038/sj.ejhg.5200946

By:

De Marco, Patrizia;
Calevo, Maria Grazia;
Moroni, Anna;
Merello, Elisa;
Raso, Alessandro;
Finnell, Richard H.;
Zhu, Huiping;
Andreussi, Luciano;
Cama, Armando;
Capra, Valeria

Publication type:

Article

Finnish and Swedish genotypes and risk of cancer in Sweden.

Published in:

European Journal of Human Genetics, 2003, v. 11, n. 3, p. 207, doi. 10.1038/sj.ejhg.5200947

By:

Hemminki, Kari;
Li, Xinjun

Publication type:

Article

Italian family with two independent mutations: 3358T/A in BRCA1 and 8756delA in BRCA2 genes.

Published in:

European Journal of Human Genetics, 2003, v. 11, n. 3, p. 210, doi. 10.1038/sj.ejhg.5200948

By:

Cortesi, Laura;
Turchetti, Daniela;
Bertoni, Chiara;
Zanocco-Marani, Tommaso;
Vinceti, Marco;
Silvestri, Chiara;
Federico, Massimo;
Silingardi, Vittorio;
Ferrari, Sergio

Publication type:

Article

Mitochondrial DNA analysis reveals diverse histories of tribal populations from India.

Published in:

European Journal of Human Genetics, 2003, v. 11, n. 3, p. 253, doi. 10.1038/sj.ejhg.5200949

By:

Cordaux, Richard;
Saha, Nilmani;
Bentley, Gillian R;
Aunger, Robert;
Sirajuddin, S M;
Stoneking, Mark

Publication type:

Article

Collagen XI sequence variations in nonsyndromic cleft palate, Robin sequence and micrognathia.

Published in:

European Journal of Human Genetics, 2003, v. 11, n. 3, p. 265, doi. 10.1038/sj.ejhg.5200950

By:

Melkoniemi, Miia;
Koillinen, Hannele;
Mannikko, Minna;
Warman, Matthew L;
Pihlajamaa, Tero;
Kaariainen, Helena;
Rautio, Jorma;
Hukki, Jyri;
Stofko, Joseph A;
Cisneros, George J;
Krakow, Deborah;
Cohn, Daniel H;
Kere, Juha;
Ala-Kokko, Leena

Publication type:

Article

Microsatellite marker association at chromosome region 2p13 in Finnish patients with preeclampsia and obstetric cholestasis suggests a common risk locus.

Published in:

European Journal of Human Genetics, 2003, v. 11, n. 3, p. 232, doi. 10.1038/sj.ejhg.5200951

By:

Laasanen, Jaana;
Hiltunen, Mikko;
Romppanen, Eeva-Liisa;
Punnonen, Kari;
Mannermaa, Arto;
Heinonen, Seppo

Publication type:

Article

Combined analysis of genomewide scans for adult height: results from the NHLBI Family Blood Pressure Program.

Published in:

European Journal of Human Genetics, 2003, v. 11, n. 3, p. 271, doi. 10.1038/sj.ejhg.5200952

By:

Wu, Xiaodong;
Cooper, Richard S;
Boerwinkle, Eric;
Turner, Stephen T;
Hunt, Steve;
Myers, Richard;
Olshen, Richard A;
Curb, David;
Zhu, Xiaofeng;
Kan, Donghui;
Luke, Amy

Publication type:

Article

ABCC6/MRP6 mutations: further insight into the molecular pathology of pseudoxanthoma elasticum.

Published in:

European Journal of Human Genetics, 2003, v. 11, n. 3, p. 215, doi. 10.1038/sj.ejhg.5200953

By:

Hu, Xiaofeng;
Plomp, Astrid;
Wijnholds, Jan;
ten Brink, Jacoline;
van Soest, Simone;
van den Born, L Ingeborgh;
Leys, Anita;
Peek, Ron;
de Jong, Paulus T V M;
Bergen, Arthur A B

Publication type:

Article

Association of NOD2 with Crohn's Disease in a homogenous Irish population.

Published in:

European Journal of Human Genetics, 2003, v. 11, n. 3, p. 237, doi. 10.1038/sj.ejhg.5200954

By:

Bairead, Emer;
Harmon, Dawn L;
Curtis, Anne M;
Kelly, Yvette;
O'Leary, Clare;
Gardner, Michelle;
Leahy, Dermot T;
Vaughan, Pat;
Keegan, Denise;
O'Morain, Colm;
O'Donoghue, Diarmuid;
Shanahan, Fergus;
Parfrey, Nollaig A;
Quane, Kathleen A

Publication type:

Article

A population-based study of the effect of the HFE C282Y and H63D mutations on iron metabolism.

Published in:

European Journal of Human Genetics, 2003, v. 11, n. 3, p. 225, doi. 10.1038/sj.ejhg.5200955

By:

Njajou, Omer T;
Houwing-Duistermaat, Jeanine J;
Osborne, Richard H;
Vaessen, Norbert;
Vergeer, Jeanette;
Heeringa, Jan;
Pols, Huibert AP;
Hofman, Albert;
van Duijn, Cornelia M

Publication type:

Article

Inverse correlation between SMN1 and SMN2 copy numbers: evidence for gene conversion from SMN2 to SMN1.

Published in:

European Journal of Human Genetics, 2003, v. 11, n. 3, p. 275, doi. 10.1038/sj.ejhg.5200957

By:

Ogino, Shuji;
Gao, Sizhen;
Leonard, Debra G B;
Paessler, Michele;
Wilson, Robert B

Publication type:

Article