Association of COL1A1 and TGFB1 Polymorphisms with Otosclerosis in a Tunisian Population (English)
- New search for: Khalfallah, A.
- New search for: Schrauwen, I.
- New search for: Mnejja, M.
- New search for: HadjKacem, H.
- New search for: Dhouib, L.
- New search for: Mosrati, M. A.
- New search for: Hakim, B.
- New search for: Lahmar, I.
- New search for: Charfeddine, I.
- New search for: Driss, N.
- New search for: Khalfallah, A.
- New search for: Schrauwen, I.
- New search for: Mnejja, M.
- New search for: HadjKacem, H.
- New search for: Dhouib, L.
- New search for: Mosrati, M. A.
- New search for: Hakim, B.
- New search for: Lahmar, I.
- New search for: Charfeddine, I.
- New search for: Driss, N.
In:
ANNALS OF HUMAN GENETICS
;
75
, 5
;
598-604
;
2011
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ISSN:
- Article (Journal) / Print
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Title:Association of COL1A1 and TGFB1 Polymorphisms with Otosclerosis in a Tunisian Population
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Contributors:Khalfallah, A. ( author ) / Schrauwen, I. ( author ) / Mnejja, M. ( author ) / HadjKacem, H. ( author ) / Dhouib, L. ( author ) / Mosrati, M. A. ( author ) / Hakim, B. ( author ) / Lahmar, I. ( author ) / Charfeddine, I. ( author ) / Driss, N. ( author )
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Published in:ANNALS OF HUMAN GENETICS ; 75, 5 ; 598-604
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Publisher:
- New search for: Blackwell Publishing Ltd
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Publication date:2011-01-01
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Size:7 pages
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ISSN:
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Type of media:Article (Journal)
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Type of material:Print
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Language:English
- New search for: 599.935
- Further information on Dewey Decimal Classification
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Classification:
DDC: 599.935 -
Source:
© Metadata Copyright the British Library Board and other contributors. All rights reserved.
Table of contents – Volume 75, Issue 5
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.
- 559
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Genetic Variants and Monoallelic Expression of Surfactant Protein‐D in Inflammatory Bowel DiseaseLin, Zhenwu / John, Gerrit / Hegarty, John P. / Berg, Arthur / Yu, Wei / Wang, Yunhua / Kelly, Ashley A. / Peterson, Blaise Z. / Poritz, Lisa S. / Floros, Joanna et al. | 2011
- 569
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Mitochondria‐Wide Association Study of Common Variants in OsteoporosisGuo, Yan / Yang, Tie‐Lin / Liu, Yao‐Zhong / Shen, Hui / Lei, Shu‐Feng / Yu, Na / Chen, Jia / Xu, Ting / Cheng, Yu / Tian, Qing et al. | 2011
- 575
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A Mutation in Cartilage Oligomeric Matrix Protein (COMP) Causes Early‐Onset Osteoarthritis in a Large Kindred StudyMu, Shu‐Chi / Lin, Yi‐Jung / Liu, Hwa‐Chang / Wu, Jer‐Yuarn / Li, Sing‐Chung / Michael Lee, Ming‐Ta / Chou, Ching‐Heng / Chen, Liang‐Kuang / Chen, Yuan‐Tsong et al. | 2011
- 584
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Heritability of Serum OsteoprotegerinKwan, Johnny S. H. / Xiao, Sumei / Bow, Cora / Cheung, Ching‐Lung / Soong, Cissy / Lau, Kam S. / Sham, Pak C. / Kung, Annie W. C. et al. | 2011
- 589
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Evidence for Age As a Modifier of Genetic Associations for Lipid LevelsDumitrescu, Logan / Brown‐Gentry, Kristin / Goodloe, Robert / Glenn, Kimberly / Yang, Wenjian / Kornegay, Nancy / Pui, Ching‐Hon / Relling, Mary V. / Crawford, Dana C. et al. | 2011
- 598
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Association of COL1A1 and TGFB1 Polymorphisms with Otosclerosis in a Tunisian PopulationKhalfallah, Ayda / Schrauwen, Isabelle / Mnejja, Malek / HadjKacem, Hassen / Dhouib, Leila / Mosrati, Mohamed Ali / Hakim, Bochra / Lahmar, Imed / Charfeddine, Ilhem / Driss, Nabil et al. | 2011
- 605
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Association between Lipoprotein‐Associated Phospholipase A2 Gene Polymorphism and Coronary Artery Disease in the Chinese Han PopulationLi, Liyun / Qi, Liping / Lv, Naqiang / Gao, Qian / Cheng, Yanmei / Wei, Yingjie / Ye, Jue / Yan, Xiaowei / Dang, Aimin et al. | 2011
- 612
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A Replication Study of the IRS1, CAPN10, TCF7L2, and PPARG Gene Polymorphisms Associated with Type 2 Diabetes in Two Different Populations of MexicoMartínez‐Gómez, Laura E. / Cruz, Miguel / Martínez‐Nava, Gabriela A. / Madrid‐Marina, Vicente / Parra, Esteban / García‐Mena, Jaime / Espinoza‐Rojo, Mónica / Estrada‐Velasco, Barbara I. / Piza‐Roman, Luis F. / Aguilera, Penelope et al. | 2011
- 621
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Peroxisome Proliferator‐Activated Receptor Delta (PPARD) Genetic Variation and Type 2 Diabetes in Middle‐Aged Chinese WomenVillegas, Raquel / Williams, Scott / Gao, Yutang / Cai, Qiuyin / Li, Honglan / Elasy, Tom / Cai, Hui / Edwards, Todd / Xiang, Yong‐Bing / Zheng, Wei et al. | 2011
- 630
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Assessing the Contribution Family Data Can Make to Case‐Control Studies of Rare VariantsCurtis, David et al. | 2011