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There are 194566 results for: content related to: Spinocerebellar ataxia type 6: Gaze-evoked and vertical nystagmus, Purkinje cell degeneration, and variable age of onset

  1. You have free access to this content
    Theoretical Problems in the Concept of Kindred

    American Anthropologist

    Volume 65, Issue 2, April 1963, Pages: 343–354, William E. Mitchell

    Version of Record online : 28 OCT 2009, DOI: 10.1525/aa.1963.65.2.02a00090

  2. The inheritance of hyperipoproteinaemia with xanthomatosis:A study of 132 kindreds

    Clinical Genetics

    Volume 9, Issue 2, February 1976, Pages: 203–233, Arvid Heiberg and Kåre Berg

    Version of Record online : 23 APR 2008, DOI: 10.1111/j.1399-0004.1976.tb01569.x

  3. Phenotype of chromosome 14–linked familial Alzheimer's disease in a large kindred

    Annals of Neurology

    Volume 36, Issue 3, September 1994, Pages: 368–378, Dr. Thomas H. Lampe, Thomas D. Bird, David Nochlin, Ellen Nemens, Steven C. Risse, S. Mark Sumi, Richard Koerker, Brie Leaird, Monna Wier and Murray A. Raskind

    Version of Record online : 8 OCT 2004, DOI: 10.1002/ana.410360308

  4. You have free access to this content
    Frameshift mutations in dentin phosphoprotein and dependence of dentin disease phenotype on mutation location

    Journal of Bone and Mineral Research

    Volume 26, Issue 4, April 2011, Pages: 873–880, Pekka Nieminen, Lisa Papagiannoulis-Lascarides, Janna Waltimo-Siren, Päivi Ollila, Sara Karjalainen, Sirpa Arte, Jaap Veerkamp, Victoria Tallon Walton, Eduard Chimenos Küstner, Tarja Siltanen, Heidi Holappa, Pirjo-Liisa Lukinmaa and Satu Alaluusua

    Version of Record online : 23 MAR 2011, DOI: 10.1002/jbmr.276

  5. GTF2I hemizygosity implicated in mental retardation in Williams syndrome: Genotype–phenotype analysis of five families with deletions in the Williams syndrome region

    American Journal of Medical Genetics Part A

    Volume 123A, Issue 1, November 15, 2003, Pages: 45–59, Colleen A. Morris, Carolyn B. Mervis, Holly H. Hobart, Ronald G. Gregg, Jacquelyn Bertrand, Gregory J. Ensing, Annemarie Sommer, Cynthia A. Moore, Robert J. Hopkin, Patricia A. Spallone, Mark T. Keating, Lucy Osborne, Kendra W. Kimberley and A. Dean Stock

    Version of Record online : 17 SEP 2003, DOI: 10.1002/ajmg.a.20496

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    THE KINDRED AND BABY BATHING IN ACADEME

    American Anthropologist

    Volume 67, Issue 4, August 1965, Pages: 977–985, WILLIAM E. MITCHELL

    Version of Record online : 28 OCT 2009, DOI: 10.1525/aa.1965.67.4.02a00070

  7. Linkage analysis of familial melanoma and chromosome 6 in 14 Australian kindreds

    Genes, Chromosomes and Cancer

    Volume 19, Issue 4, August 1997, Pages: 241–249, E. A. Holland, S. C. Beaton, R. F. Kefford and G. J. Mann

    Version of Record online : 7 DEC 1998, DOI: 10.1002/(SICI)1098-2264(199708)19:4<241::AID-GCC6>3.0.CO;2-X

  8. Knowledge of genetics and attitudes toward genetic testing in two hereditary ataxia (SCA 1) Kindreds

    American Journal of Medical Genetics

    Volume 54, Issue 3, 15 September 1994, Pages: 242–248, Dr. Martha A. Nance, Ellen A. Sevenich and Lawrence J. Schut

    Version of Record online : 7 JUN 2005, DOI: 10.1002/ajmg.1320540310

  9. Dopaminergic function in familial Parkinson's disease: A clinical and 18F-dopa positron emission tomography study

    Annals of Neurology

    Volume 41, Issue 2, February 1997, Pages: 222–229, Dr P. Piccini, P. K. Morrish, N. Turjanski, G. V. Sawle, D. J. Burn, R. A. Weeks, M. H. Mark, D. M. Maraganore, A. J. Lees and D. J. Brooks

    Version of Record online : 8 OCT 2004, DOI: 10.1002/ana.410410213

  10. Concordance of disease form in kindreds ascertained through affected individuals

    Statistics in Medicine

    Volume 21, Issue 13, 15 July 2002, Pages: 1887–1897, Melodie Winawer, Ruth Ottman and Daniel Rabinowitz

    Version of Record online : 7 JUN 2002, DOI: 10.1002/sim.988

  11. Polymorphism of apolipoprotein E

    Clinical Genetics

    Volume 15, Issue 1, January 1979, Pages: 37–62, G. Utermann, K. H. Vogelberg, A. Steinmetz, W. Schoenborn, N. Pruin, M. Jaeschke, M. Hees and H. Canzler

    Version of Record online : 23 APR 2008, DOI: 10.1111/j.1399-0004.1979.tb02027.x

  12. Analysis of problems and barriers of small food and kindred products processors

    Agribusiness

    Volume 7, Issue 4, July 1991, Pages: 311–325, Steven J. Torok, Alan Schroeder and Dale J. Menkhaus

    Version of Record online : 9 MAR 2006, DOI: 10.1002/1520-6297(199107)7:4<311::AID-AGR2720070402>3.0.CO;2-1

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    Patrilineal Descent and Personal Kindred in Japan

    American Anthropologist

    Volume 65, Issue 6, December 1963, Pages: 1328–1341, HARUMI BEFU

    Version of Record online : 28 OCT 2009, DOI: 10.1525/aa.1963.65.6.02a00070

  14. Clinical manifestations in a large hereditary hemorrhagic telangiectasia (HHT) type 2 kindred

    American Journal of Medical Genetics

    Volume 93, Issue 4, 14 August 2000, Pages: 320–327, Jamie E. McDonald, Franklin J. Miller, Stephanie E. Hallam, Lesa Nelson, Douglas A. Marchuk and Kenneth J. Ward

    Version of Record online : 11 AUG 2000, DOI: 10.1002/1096-8628(20000814)93:4<320::AID-AJMG12>3.0.CO;2-R

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    The Structure of the Sinhalese Kindred: A Re-Examination of the Dravidian Terminology

    American Anthropologist

    Volume 64, Issue 3, June 1962, Pages: 548–575, NUR YALMAN

    Version of Record online : 28 OCT 2009, DOI: 10.1525/aa.1962.64.3.02a00060

  16. CDKN2A (P16INK4a) and CDK4 mutation analysis in 131 Australian melanoma probands: Effect of family history and multiple primary melanomas

    Genes, Chromosomes and Cancer

    Volume 25, Issue 4, August 1999, Pages: 339–348, Elizabeth A. Holland, Helen Schmid, Richard F. Kefford and Graham J. Mann

    Version of Record online : 7 JUL 1999, DOI: 10.1002/(SICI)1098-2264(199908)25:4<339::AID-GCC5>3.0.CO;2-H

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    An analysis of 5 “stomach cancer families” in the State of Utah

    Cancer

    Volume 14, Issue 5, September/October 1961, Pages: 1005–1016, Charles M. Woolf and E. Arnold Isaacson

    Version of Record online : 23 JUN 2006, DOI: 10.1002/1097-0142(196109/10)14:5<1005::AID-CNCR2820140515>3.0.CO;2-Z

  18. Familial medullary thyroid carcinoma without associated endocrinopathies: A distinct clinical entity

    British Journal of Surgery

    Volume 73, Issue 4, April 1986, Pages: 278–281, Mr J. R. Farndon, G. S. Leightt, W. G. Dilley, S. B. Baylin, R. C. Smallridge, T. S. Harrison and S. A. Wells Jr

    Version of Record online : 7 DEC 2005, DOI: 10.1002/bjs.1800730411

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    Metabolism of C4 and linkage analysis in a kindred with hereditary incomplete C4 deficiency

    Arthritis & Rheumatism

    Volume 30, Issue 8, August 1987, Pages: 919–926, Jeffrey J. Wisnieski, Michael H. Nathanson, Jeanne E. Anderson, Alvin E. Davis Iii, Chester A. Alper and George B. Naff

    Version of Record online : 29 NOV 2005, DOI: 10.1002/art.1780300812

  20. Frontotemporal dementia and parkinsonism linked to chromosome 17: A consensus conference

    Annals of Neurology

    Volume 41, Issue 6, June 1997, Pages: 706–715, Dr Norman L. Foster, Kirk Wilhelmsen, Anders A. F. Sima, Margaret Z. Jones, Constance J. D'Amato and Sid Gilman

    Version of Record online : 8 OCT 2004, DOI: 10.1002/ana.410410606