Clinical Genetics

Cover image for Clinical Genetics

June 1998

Volume 53, Issue 6

Pages 423–505

  1. Mini Review

    1. Top of page
    2. Mini Review
    3. HotSpots
    4. Original Article
    5. Short Report
    6. Short Report on DNA Marker at Candidate Locus
    7. Announcements
    1. Recessive or dominant? Reclassification in the molecular age (pages 423–425)

      Joël Zlotogora

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1998.tb02587.x

  2. HotSpots

    1. Top of page
    2. Mini Review
    3. HotSpots
    4. Original Article
    5. Short Report
    6. Short Report on DNA Marker at Candidate Locus
    7. Announcements
  3. Original Article

    1. Top of page
    2. Mini Review
    3. HotSpots
    4. Original Article
    5. Short Report
    6. Short Report on DNA Marker at Candidate Locus
    7. Announcements
    1. Evaluation of a clinically applicable mutation screening technique for genetic diagnosis of familial hypercholesterolemia and familial defective apolipoprotein B (pages 433–439)

      Henrik Nissen, Annebirthe B. Hansen, Per Guldberg, Torben S. Hansen, Niels E. Petersen and Mogens Harder

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1998.tb02591.x

    2. Ehlers-Danlos syndrome and type III collagen abnormalities: a variable clinical (pages 440–446)

      BCJ Hamel, G. Pals, CHAM Engels, E. van den Akker, GHJ Boers, PWJ van Dongen and PM Steijlen

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1998.tb02592.x

    3. Physician knowledge and attitudes towards molecular genetic (DNA) testing of their patients (pages 447–455)

      Alasdair Hunter, Peter Wright, Mario Cappelli, Ann Kasaboski and Linda Surh

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1998.tb02593.x

  4. Short Report

    1. Top of page
    2. Mini Review
    3. HotSpots
    4. Original Article
    5. Short Report
    6. Short Report on DNA Marker at Candidate Locus
    7. Announcements
    1. Exploring gene—gene interactions in the etiology of neural tube defects (pages 456–459)

      Lorenzo D. Botto and Pierpaolo Mastroiacovo

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1998.tb02594.x

    2. Aortic root dilatation in Ehlers-Danlos syndrome types I, II and III A report of five cases (pages 460–465)

      George E. Tiller, Suzanne B. Cassidy, Christine Wensel and Richard J. Wenstrup

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1998.tb02595.x

    3. A new case of Ambras syndrome associated with a paracentric inversion (8) (q12; q22) (pages 466–468)

      R. Balducci, V. Toscano, B. Tedeschi, A. Mangiantini, R. Toscano, C. Galasso, S. Cianfarani and B. Boscherini

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1998.tb02596.x

    4. Presenilin 1 Met146Leu variant due to an A&T transversion in an early-onset familial Alzheimer's disease pedigree from Argentina (pages 469–473)

      Laura Morelli, María I. Prat, Efrat Levy, Carlos A. Mangone and Eduardo M. Castaño

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1998.tb02597.x

    5. A deletion involving exons 2–4 in the iduronate-2-sulfatase gene of a patient with intermediate Hunter syndrome (pages 474–477)

      Gloria Bonuccelli, Stefano Regis, Mirella Filocamo, Fabio Corsolini, Francesco Caroli and Rosanna Gatti

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1998.tb02598.x

    6. Detection of factor V Leiden mutation in severe pre-eclamptic Hungarian women (pages 478–481)

      Bálint Nagy, Tamás Tóth, János Rigó Jr, István Karádi, László Romics and Zoltán Papp

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1998.tb02599.x

    7. Characterization of a novel mutation in exon 10 of the adrenoleukodystrophy gene (pages 482–487)

      Andreas Holzinger, Esther Maier, Sylvia Stöckler-lpsiroglu, Andreas Braun and Adelbert A. Roscher

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1998.tb02600.x

    8. Prenatal identification of de novo marker chromosomes using micro-FISH approach (pages 490–496)

      Jia Xu, Chin-To Fong, Edward Cedrone1, Julie Sullivan and Nancy Wang

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1998.tb02602.x

    9. Sclerosteosis: report of a case in a black African man (pages 497–501)

      Paolo Tacconi, Paola Ferrigno, Luigi Cocco, Antonino Carinas, Giorgio Tamburini, Paolo Bergonzi and Marcello Giagheddu

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1998.tb02603.x

  5. Short Report on DNA Marker at Candidate Locus

    1. Top of page
    2. Mini Review
    3. HotSpots
    4. Original Article
    5. Short Report
    6. Short Report on DNA Marker at Candidate Locus
    7. Announcements
    1. Rsal and Mael intragenic RFLPs in the human HERG gene (page 504)

      D. Fung, L. Zhang, J. French, B. Bailey and RJ Trent

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1998.tb02605.x

  6. Announcements

    1. Top of page
    2. Mini Review
    3. HotSpots
    4. Original Article
    5. Short Report
    6. Short Report on DNA Marker at Candidate Locus
    7. Announcements
    1. Announcements (page 505)

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1998.tb02606.x

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