American Journal of Medical Genetics

Cover image for American Journal of Medical Genetics

19 June 1995

Volume 60, Issue 3

Pages fmi–fmi, 179–262

Currently known as: American Journal of Medical Genetics Part A

  1. Masthead

    1. Top of page
    2. Masthead
    3. Articles
    4. Letter to the Editor
    1. Masthead (page fmi)

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320600301

  2. Articles

    1. Top of page
    2. Masthead
    3. Articles
    4. Letter to the Editor
    1. Type I bipolar disorder associated with a fragile site on chromosome 1 (pages 179–182)

      G. Turecki, Prof. M. de A. C. Smith and J. J. Mari

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320600302

    2. Polymorphism and genetic mapping of the human oxytocin receptor gene on chromosome 3 (pages 183–187)

      Stefano Michelini, Margrit Urbanek, Michael Dean and David Goldman

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320600303

    3. Spinocerebellar degeneration and cerebral hypomyelination in a family (pages 188–191)

      Sansnee Chatkupt, Leo J. Wolansky, Annette Jotkowitz, Ling Y. Shih and Stuart D. Cook

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320600304

    4. Automated linkage analysis in psychiatric disorders (pages 192–198)

      Dr. L. He, D. C. Mansfield, A. F. Brown, D. K. Green, S. W. Morris, D. M. St. Clair, W. J. Muir, A. Maclean, A. F. Wright and D. H. R. Blackwood

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320600305

    5. DRD4 dopamine receptor genotype and CSF monoamine metabolites in Finnish alcoholics and controls (pages 199–205)

      M. D. Adamson, J. Kennedy, A. Petronis, M. Dean, M. Virkkunen, M. Linnoila and D. Goldman

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320600306

    6. Familial cosegregation of manic-depressive illness and a form of hereditary cerebellar ataxia (pages 206–209)

      Dr. José Fernández Piqueras, Javier Santos, Guillermo Visedo, Ignacio Pérez de Castro, Rosa Puertollano, Julieta Montejo, Cristina Ramo Tello and Jesús Valle

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320600307

    7. Central pontine myelinolysis as a complication of partial ornithine carbamoyl transferase deficiency (pages 210–213)

      Lisa R. Mattson, Noralane M. Lindor, Deborah H. Goldman, Jeffrey T. Goodwin, Robert V. Groover and Jerry Vockley

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320600308

    8. Characteristics of familial aggregation in early-onset Alzheimer's disease: Evidence of subgroups (pages 221–227)

      Dr. D. Campion, M. Martinez, D. Hannequin, A. Brice, C. Thomas-Anterion, A. Michon, M. C. Babron, B. Dubois, Y. Goas, A. Jaillard-Serradt, F. Ledoze, F. Pasquier, M. Puel, M. A. Zimmerman, M. Bellis, J. Mallet, Y. Agid and F. Clerget-Darpoux

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320600310

    9. Structural change in dopamine D2 receptor gene in a patient with neuroleptic malignant syndrome (pages 228–230)

      Anca Ram, Qiuhe Cao, Paul E. Keck Jr., Harrison G. Pope Jr., Koichi Otani, Gerard Addonizio, Susan L. McElroy, Sunao Kaneko, Michaela Redlichova, Elliot S. Gershon and Pablo V. Gejman

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320600311

    10. Search for a gene predisposing to manic-depression on chromosome 21 (pages 231–233)

      William Byerley, John Holik, Mark Hoff and Hilary Coon

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320600312

    11. Possible association between the dopamine D3 receptor gene and bipolar affective disorder (pages 234–237)

      Dr. Abbas Parsian, Sumitra Chakraverty and Richard D. Todd

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320600313

    12. Magnetic resonance imaging of cerebral anomalies in subjects with resistance to thyroid hormone (pages 238–243)

      Christiana M. Leonard, Pedro Martinez, Bruce D. Weintraub and Dr. Peter Hauser

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320600314

    13. Towards the finer mapping of facioscapulohumeral muscular dystrophy at 4q35: Construction of a laser microdissection library (pages 244–251)

      Dr. M. Upadhyaya, M. Osborn, J. Maynard, M. Altherr, J. Ikeda and P. S. Harper

      Version of Record online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320600315

    14. Schizophrenia: A genome scan targets chromosomes 3p and 8p as potential sites of susceptibility genes (pages 252–260)

      Ann E. Pulver, Virginia K. Lasseter, Laura Kasch, Paula Wolyniec, Gerald Nestadt, Jean-Louis Blouin, Michelle Kimberland, Robert Babb, Sophia Vourlis, Haiming Chen, Maria Lalioti, Michael A. Morris, Maria Karayiorgou, Jurg Ott, Deborah Meyers, Stylianos E. Antonarakis, David Housman and Haig H. Kazazian

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320600316

  3. Letter to the Editor

    1. Top of page
    2. Masthead
    3. Articles
    4. Letter to the Editor
    1. Clinical, cytogenetic, and molecular diagnosis of Angelman syndrome: Estimated prevalence rate in a Danish county (pages 261–262)

      Michael B. Petersen, Karen Brøndum-Nielsen, Lars Kjærsgård Hansen and Karl Wulff

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320600317

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