Mitochondrial DNA Diversity in Indigenous Populations of the Southern Extent of Siberia, and the Origins of Native American Haplogroups (English)
- New search for: Starikovskaya, Elena B.
- New search for: Sukernik, Rem I.
- New search for: Derbeneva, Olga A.
- New search for: Volodko, Natalia V.
- New search for: Ruiz‐Pesini, Eduardo
- New search for: Torroni, Antonio
- New search for: Brown, Michael D.
- New search for: Lott, Marie T.
- New search for: Hosseini, Seyed H.
- New search for: Huoponen, Kirsi
- New search for: Wallace, Douglas C.
- New search for: Starikovskaya, Elena B.
- New search for: Sukernik, Rem I.
- New search for: Derbeneva, Olga A.
- New search for: Volodko, Natalia V.
- New search for: Ruiz‐Pesini, Eduardo
- New search for: Torroni, Antonio
- New search for: Brown, Michael D.
- New search for: Lott, Marie T.
- New search for: Hosseini, Seyed H.
- New search for: Huoponen, Kirsi
- New search for: Wallace, Douglas C.
In:
Annals of Human Genetics
;
69
, 1
;
67-89
;
2005
- Article (Journal) / Electronic Resource
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Title:Mitochondrial DNA Diversity in Indigenous Populations of the Southern Extent of Siberia, and the Origins of Native American Haplogroups
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Contributors:Starikovskaya, Elena B. ( author ) / Sukernik, Rem I. ( author ) / Derbeneva, Olga A. ( author ) / Volodko, Natalia V. ( author ) / Ruiz‐Pesini, Eduardo ( author ) / Torroni, Antonio ( author ) / Brown, Michael D. ( author ) / Lott, Marie T. ( author ) / Hosseini, Seyed H. ( author ) / Huoponen, Kirsi ( author )
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Published in:Annals of Human Genetics ; 69, 1 ; 67-89
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Publisher:
- New search for: Blackwell Science Ltd
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Publication date:2005-01-01
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Size:23 pages
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ISSN:
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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
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Keywords:
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Source:
Table of contents – Volume 69, Issue 1
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.
- 1
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Phenotype Severity and Genetic Variation at the Disease Locus: An Investigation of Nail Dysplasia in the Nail Patella SyndromeDunston, J. A. / Lin, S. / Park, J. W. / Malbroux, M. / McIntosh, I. et al. | 2005
- 9
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Double Heterozygosity with Mutations Involving both the GJB2 and GJB6 Genes is a Possible, but very Rare, Cause of Congenital Deafness in the Czech PopulationSeeman, P. / Bendová, O. / Rašková, D. / Malíková, M. / Groh, D. / Kabelka, Z. et al. | 2005
- 15
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Comprehensive Cystic Fibrosis Mutation Epidemiology and Haplotype Characterization in a Southern Italian PopulationCastaldo, G. / Polizzi, A. / Tomaiuolo, R. / Cazeneuve, C. / Girodon, E. / Santostasi, T. / Salvatore, D. / Raia, V. / Rigillo, N. / Goossens, M. et al. | 2005
- 25
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The Contribution of Genetic and Environmental Factors to Quantitative Variability of Erythrocyte Membrane Proteins in Primary HypotensionIvanov, V. P. / Polonikov, A. V. / Solodilova, M. A. et al. | 2005
- 36
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b2-Adrenergic Receptor Gene Variations Associated with Stage-2 Hypertension in Northern Han ChineseGe, D. / Huang, J. / He, J. / Li, B. / Duan, X. / Chen, R. / Gu, D. et al. | 2005
- 36
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β2‐Adrenergic Receptor Gene Variations Associated with Stage‐2 Hypertension in Northern Han ChineseGe, D. / Huang, J. / He, J. / Li, B. / Duan, X. / Chen, R. / Gu, D. et al. | 2005
- 45
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Linkage Analysis of Chromosome 1 with Essential Hypertension and Blood Pressure Quantitative Traits in Chinese FamiliesGe, D. / Huang, J. / Yang, W. / Zhao, J. / Shen, Y. / Qiang, B. / Gu, D. et al. | 2005
- 55
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Genetic Heterogeneity of Beta Thalassemia in Lebanon Reflects Historic and Recent Population MigrationMakhoul, N. J. / Wells, R. S. / Kaspar, H. / Shbaklo, H. / Taher, A. / Chakar, N. / Zalloua, P. A. et al. | 2005
- 67
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Mitochondrial DNA Diversity in Indigenous Populations of the Southern Extent of Siberia, and the Origins of Native American HaplogroupsStarikovskaya, Elena B. / Sukernik, Rem I. / Derbeneva, Olga A. / Volodko, Natalia V. / Ruiz‐Pesini, Eduardo / Torroni, Antonio / Brown, Michael D. / Lott, Marie T. / Hosseini, Seyed H. / Huoponen, Kirsi et al. | 2005
- 90
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Genetic Association Studies in Complex Disease: Disentangling Additional Predisposing Loci from Associated Neutral Loci Using a Constrained ‐ Permutation ApproachSpijker, G.T. / Nolte, I.M. / Jansen, R.C. / Te Meerman, G.J. et al. | 2005
- 102
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Fine Mapping Functional Sites or Regions from Case‐Control Data Using Haplotypes of Multiple Linked SNPsCheng, Rong / Ma, Jennie Z. / Elston, Robert C. / Li, Ming D. et al. | 2005
- 113
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Linkage Analysis of Affected Sib Pairs Allowing for Parent‐of‐Origin EffectsWu, Chih‐Chieh / Shete, Sanjay / Amos, Christopher I. et al. | 2005
- 127
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The use of Allelic Expression Differences to Ascertain Functional Polymorphisms Acting in cis: Analysis of MMP1 Transcripts in Normal Lung TissueHeighway, J. / Bowers, N. L. / Smith, S. / Betticher, D. C. / Santibáñez Koref, M. F. et al. | 2005
- 134
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Corrigendum| 2005