The origin and spread of the HFE-C282Y haemochromatosis mutation (English)
- New search for: Distante, S.
- New search for: Robson, K. J. H.
- New search for: Graham-Campbell, J.
- New search for: Arnaiz-Villena, A.
- New search for: Brissot, P.
- New search for: Worwood, Mark
- New search for: Distante, S.
- New search for: Robson, K. J. H.
- New search for: Graham-Campbell, J.
- New search for: Arnaiz-Villena, A.
- New search for: Brissot, P.
- New search for: Worwood, Mark
In:
Human Genetics
;
115
, 4
; 269-279
;
2004
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ISSN:
- Article (Journal) / Electronic Resource
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Title:The origin and spread of the HFE-C282Y haemochromatosis mutation
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Contributors:Distante, S. ( author ) / Robson, K. J. H. ( author ) / Graham-Campbell, J. ( author ) / Arnaiz-Villena, A. ( author ) / Brissot, P. ( author ) / Worwood, Mark ( author )
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Published in:Human Genetics ; 115, 4 ; 269-279
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Publisher:
- New search for: Springer-Verlag
- New search for: Springer
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Place of publication:Berlin
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Publication date:2004
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ISSN:
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ZDBID:
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DOI:
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Type of media:Article (Journal)
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Type of material:Electronic Resource
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Language:English
- New search for: 44.48
- Further information on Basic classification
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Keywords:
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Classification:
BKL: 44.48 Medizinische Genetik -
Source:
Table of contents – Volume 115, Issue 4
The tables of contents are generated automatically and are based on the data records of the individual contributions available in the index of the TIB portal. The display of the Tables of Contents may therefore be incomplete.
- 269
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The origin and spread of the HFE-C282Y haemochromatosis mutationDistante, S. / Robson, K. J. H. / Graham-Campbell, J. / Arnaiz-Villena, A. / Brissot, P. / Worwood, Mark et al. | 2004
- 280
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Inheritance mode of multiple sclerosis: the effect of HLA class II alleles is stronger than additiveBoon, Maartje / Nolte, Ilja M. / De Keyser, Jacques / Buys, Charles H. C. M. / te Meerman, Gerard J. et al. | 2004
- 285
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Comparison of the genomic structure and variation in the two human sodium-dependent vitamin C transporters, SLC23A1 and SLC23A2Eck, Peter / Erichsen, Hans Christian / Taylor, James G. / Yeager, Meredith / Hughes, Austin L. / Levine, Mark / Chanock, Stephen J. et al. | 2004
- 295
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Variations in the C3, C3a receptor, and C5 genes affect susceptibility to bronchial asthmaHasegawa, Koichi / Tamari, Mayumi / Shao, Chenchen / Shimizu, Makiko / Takahashi, Naomi / Mao, Xiao-Quan / Yamasaki, Akiko / Kamada, Fumiaki / Doi, Satoru / Fujiwara, Hiroshi et al. | 2004
- 302
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CHX10 mutations cause non-syndromic microphthalmia/anophthalmia in Arab and Jewish kindredsBar-Yosef, Udy / Abuelaish, Izzeldin / Harel, Tamar / Hendler, Neta / Ofir, Rivka / Birk, Ohad S. et al. | 2004
- 310
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Association between evolutionary history of angiotensinogen haplotypes and plasma levelsFejerman, Laura / Bouzekri, Nourdine / Wu, Xiaodong / Adeyemo, Adebowale / Luke, Amy / Zhu, Xiaofeng / Ward, Ryk / Cooper, Richard S. et al. | 2004
- 319
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Genomic rearrangements at the IGHMBP2 gene locus in two patients with SMARD1Guenther, Ulf P. / Schuelke, Markus / Bertini, Enrico / D’Amico, Adele / Goemans, Nathalie / Grohmann, Katja / Hübner, Christoph / Varon, Raymonda et al. | 2004
- 327
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Concurrent analysis of loss of heterozygosity (LOH) and copy number abnormality (CNA) for oral premalignancy progression using the Affymetrix 10K SNP mapping arrayZhou, Xiaofeng / Mok, Samuel C. / Chen, Zugen / Li, Yang / Wong, David T. W. et al. | 2004
- 331
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Gender- and age-specific contributions of additional DNA sequence variation in the 5′ regulatory region of the APOE gene to prediction of measures of lipid metabolismFrikke-Schmidt, Ruth / Sing, Charles F. / Nordestgaard, Børge G. / Tybjærg-Hansen, Anne et al. | 2004
- 346
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E.A. Carlson (ed) Mendel’s Legacy: the origin of classical genetics (2004)Harper, Peter S. et al. | 2004
- 347
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Mutations| 2004