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Annals of Human Genetics

Cover image for Vol. 71 Issue 3

May 2007

Volume 71, Issue 3

Pages 281–420

  1. Original Articles

    1. Top of page
    2. Original Articles
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      A Novel Genetic Study of Chinese Families with Autosomal Recessive Retinitis Pigmentosa (pages 281–294)

      M. M. Abd El-Aziz, M. F. El-Ashry, W. M. Chan, K. L. Chong, I. Barragan, G. Antiñolo, C. P. Pang and S. S. Bhattacharya

      Version of Record online: 29 NOV 2006 | DOI: 10.1111/j.1469-1809.2006.00333.x

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      The Relationship Between CAG Repeat Length and Age of Onset Differs for Huntington's Disease Patients with Juvenile Onset or Adult Onset (pages 295–301)

      J. Michael Andresen, Javier Gayán, Luc Djoussé, Simone Roberts, Denise Brocklebank, Stacey S. Cherny, The US-Venezuela Collaborative Research Group, The HD MAPS Collaborative Research Group, Lon R. Cardon, James F. Gusella, Marcy E. MacDonald, Richard H. Myers, David E. Housman and Nancy S. Wexler

      Version of Record online: 19 DEC 2006 | DOI: 10.1111/j.1469-1809.2006.00335.x

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      Association of a Common Interferon Regulatory Factor 5 (IRF5) Variant with Increased Risk of Systemic Lupus Erythematosus (SLE) (pages 308–311)

      F. Y. K. Demirci, S. Manzi, R. Ramsey-Goldman, R. L. Minster, M. Kenney, P. S. Shaw, C. M. Dunlop-Thomas, A. H. Kao, E. Rhew, F. Bontempo, C. Kammerer and M. I. Kamboh

      Version of Record online: 12 DEC 2006 | DOI: 10.1111/j.1469-1809.2006.00336.x

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      Correlation between single nucleotide polymorphisms in a calprotectin subunit gene and risk of periodontitis in a Chinese population (pages 312–324)

      QiYan Li, HuanXin Meng, Li Zhang, Li Xu, ZhiBin Chen, Dong Shi, XiangHui Feng, XiaoLing Zhu, HongShan Zhao and CaiFang Cao

      Version of Record online: 27 OCT 2006 | DOI: 10.1111/j.1469-1809.2006.00326.x

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      Common Polymorphisms in the CACNA1H Gene Associated with Childhood Absence Epilepsy in Chinese Han Population (pages 325–335)

      J. Liang, Y. Zhang, Y. Chen, J. Wang, H. Pan, H. Wu, K. Xu, X. Liu, Y. Jiang, Y. Shen and X. Wu

      Version of Record online: 22 NOV 2006 | DOI: 10.1111/j.1469-1809.2006.00332.x

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      Congenital Disorder of Glycosylation Type Ia: Searching for the Origin of Common Mutations in PMM2 (pages 348–353)

      D. Quelhas, R. Quental, L. Vilarinho, A. Amorim and L. Azevedo

      Version of Record online: 12 DEC 2006 | DOI: 10.1111/j.1469-1809.2006.00334.x

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      The Gagauz, a Linguistic Enclave, are not a Genetic Isolate (pages 379–389)

      Ivan Nasidze, Dominique Quinque, Irina Udina, Svetlana Kunizheva and Mark Stoneking

      Version of Record online: 28 NOV 2006 | DOI: 10.1111/j.1469-1809.2006.00330.x

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