Clinical Genetics

Cover image for Clinical Genetics

January 1991

Volume 39, Issue 1

Pages 1–80

  1. Original Article

    1. Top of page
    2. Original Article
    3. Case Report
    4. Short Communication
    5. Announcement
    1. Coronary artery disease and apolipoprotein A-I/C-III gene polymorphism: a study of Saudi Arabians (pages 1–5)

      Klaus Johansen, Bruce Dunn, Jenny C. Y. Tan, Aaron A. A. Kwaasi, Antek Skotnicki and Mary Skotnickl

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1991.tb02978.x

    2. A new transthyretin variant from a patient with familial amyloidotic polyneuropathy has asparagine substituted for histidine at position 90 (pages 6–12)

      James C. Skare, Jeffrey M. Milunsky, Aubrey Milunsky, Ilze B. Skare, Alan S. Cohen and Martha Skinner

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1991.tb02979.x

    3. Glyceryl ethers in peroxisomal disease (pages 13–25)

      A. Poulos, A. Bankier, K. Beckman, D. Johnson, E. F. Robertson, P. Sharp, L. Sheffield, H. Singh, S. Usher and G. Wise

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1991.tb02980.x

    4. Detection of mitochondrial DNA deletions in blood using the polymerase chain reaction: non-invasive diagnosis of mitochondrial myopathy (pages 33–38)

      J. Poulton, M. E. Deadman, D. M. Turnbull, B. Lake and R. M. Gardiner

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1991.tb02982.x

    5. Age of onset in vitiligo: relationship with HLA supratypes (pages 48–54)

      O. Finco, M. Cuccia, M. Martinetti, G. Ruberto, G. Orecchia and G. Rabbiosi

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1991.tb02984.x

  2. Case Report

    1. Top of page
    2. Original Article
    3. Case Report
    4. Short Communication
    5. Announcement
    1. Inv dup (8) (p21.1 [RIGHTWARDS ARROW] 22.1): further case report and a new hypothesis on the origin of the chromosome abnormality (pages 55–59)

      Marino Gorinati, Daniele Caufin, Antonella Minelli, Luigi Memo, Gianfranco Gaspardo and Andrea Dodero

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1991.tb02985.x

    2. Tetrasomy 9p: an emerging syndrome (pages 60–64)

      S. M. Jalal, Mary K. Kukolich, Mary Garcia, Toni R. Benjamin and Donald W. Day

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1991.tb02986.x

    3. Recurrent neuroleptic malignant syndrome associated with inv dup(15) and mental retardation (pages 65–67)

      Arthur L. Lazarus, Kenneth E. Moore and Nancy B. Spinner

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1991.tb02987.x

    4. Pigmentary dysplasias in long survivors with mosaic trisomy 18: report of two cases (pages 68–74)

      I. Murano, H. Ohashi, M. Tsukahara, H. Tonoki, F. Okino, M. Atsumi and T. Kajii

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1991.tb02988.x

  3. Short Communication

    1. Top of page
    2. Original Article
    3. Case Report
    4. Short Communication
    5. Announcement
    1. Dizygotic twins concordant for truncus arteriosus (pages 75–79)

      Michael J. Lang, David J. Aughton, Thomas W. Riggs, Magdy P. Milad and Leslie G. Biesecker

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1991.tb02989.x

  4. Announcement

    1. Top of page
    2. Original Article
    3. Case Report
    4. Short Communication
    5. Announcement
    1. Announcement (page 80)

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1991.tb02990.x

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