Works matching IS 03406717 AND DT 2004 AND VI 115 AND IP 4

Results: 11

E.A. Carlson (ed) Mendel’s Legacy: the origin of classical genetics (2004).
Published in:
2004
By:
- Harper, Peter
Publication type:
Book Review
CHX10mutations cause non-syndromic microphthalmia/anophthalmia in Arab and Jewish kindreds.
Published in:
Human Genetics, 2004, v. 115, n. 4, p. 302, doi. 10.1007/s00439-004-1154-2
By:
- Bar-Yosef, Udy;
- Abuelaish, Izzeldin;
- Harel, Tamar;
- Hendler, Neta;
- Ofir, Rivka;
- Birk, Ohad
Publication type:
Article
Association between evolutionary history of angiotensinogen haplotypes and plasma levels.
Published in:
Human Genetics, 2004, v. 115, n. 4, p. 310, doi. 10.1007/s00439-004-1141-7
By:
- Fejerman, Laura;
- Bouzekri, Nourdine;
- Wu, Xiaodong;
- Adeyemo, Adebowale;
- Luke, Amy;
- Zhu, Xiaofeng;
- Ward, Ryk;
- Cooper, Richard
Publication type:
Article
Variations in the C3, C3a receptor, and C5 genes affect susceptibility to bronchial asthma.
Published in:
Human Genetics, 2004, v. 115, n. 4, p. 295, doi. 10.1007/s00439-004-1157-z
By:
- Hasegawa, Koichi;
- Tamari, Mayumi;
- Shao, Chenchen;
- Shimizu, Makiko;
- Takahashi, Naomi;
- Mao, Xiao-Quan;
- Yamasaki, Akiko;
- Kamada, Fumiaki;
- Doi, Satoru;
- Fujiwara, Hiroshi;
- Miyatake, Akihiko;
- Fujita, Kimie;
- Tamura, Gen;
- Matsubara, Yoichi;
- Shirakawa, Taro;
- Suzuki, Yoichi
Publication type:
Article
Concurrent analysis of loss of heterozygosity (LOH) and copy number abnormality (CNA) for oral premalignancy progression using the Affymetrix 10K SNP mapping array.
Published in:
Human Genetics, 2004, v. 115, n. 4, p. 327, doi. 10.1007/s00439-004-1163-1
By:
- Zhou, Xiaofeng;
- Mok, Samuel;
- Chen, Zugen;
- Li, Yang;
- Wong, David
Publication type:
Article
The origin and spread of theHFE-C282Y haemochromatosis mutation.
Published in:
Human Genetics, 2004, v. 115, n. 4, p. 269, doi. 10.1007/s00439-004-1152-4
By:
- Distante, S.;
- Robson, K.;
- Graham-Campbell, J.;
- Arnaiz-Villena, A.;
- Brissot, P.;
- Worwood, Mark
Publication type:
Article
Genomic rearrangements at theIGHMBP2gene locus in two patients with SMARD1.
Published in:
Human Genetics, 2004, v. 115, n. 4, p. 319, doi. 10.1007/s00439-004-1156-0
By:
- Guenther, Ulf;
- Schuelke, Markus;
- Bertini, Enrico;
- D’Amico, Adele;
- Goemans, Nathalie;
- Grohmann, Katja;
- Hübner, Christoph;
- Varon, Raymonda
Publication type:
Article
Inheritance mode of multiple sclerosis: the effect ofHLAclass II alleles is stronger than additive.
Published in:
Human Genetics, 2004, v. 115, n. 4, p. 280, doi. 10.1007/s00439-004-1169-8
By:
- Boon, Maartje;
- Nolte, Ilja;
- Keyser, Jacques;
- Buys, Charles;
- Meerman, Gerard
Publication type:
Article
Gender- and age-specific contributions of additional DNA sequence variation in the 5' regulatory region of theAPOEgene to prediction of measures of lipid metabolism.
Published in:
Human Genetics, 2004, v. 115, n. 4, p. 331, doi. 10.1007/s00439-004-1165-z
By:
- Frikke-Schmidt, Ruth;
- Sing, Charles;
- Nordestgaard, Børge;
- Tybjærg-Hansen, Anne
Publication type:
Article
Comparison of the genomic structure and variation in the two human sodium-dependent vitamin C transporters,SLC23A1andSLC23A2.
Published in:
Human Genetics, 2004, v. 115, n. 4, p. 285, doi. 10.1007/s00439-004-1167-x
By:
- Eck, Peter;
- Erichsen, Hans;
- Taylor, James;
- Yeager, Meredith;
- Hughes, Austin;
- Levine, Mark;
- Chanock, Stephen
Publication type:
Article
Mutations.
Published in:
Human Genetics, 2004, v. 115, n. 4, p. 347, doi. 10.1007/s00439-004-1161-3
Publication type:
Article