Clinical Genetics

Cover image for Clinical Genetics

September 1997

Volume 52, Issue 3

Pages 135–198

  1. Original Article

    1. Top of page
    2. Original Article
    3. Case Report
    4. Short Communication
    5. Short Report on DNA Marker at Candidate Locus
    6. Letter to the Editor
    1. A study of the cognitive and psychological profile in 16 children with congenital or juvenile myotonic dystrophy (pages 135–141)

      J. Steyaert, S. Umans, D. Willekens, E. Legius, E. Pijkels, C. de Die-Smulders, H. Van den Berghe and J-P. Fryns

      Article first published online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1997.tb02533.x

    2. Consanguineous marriage and its clinical consequences in migrants to Australia (pages 142–146)

      J. Nelson, M. Smith and A. H. Bittles

      Article first published online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1997.tb02534.x

    3. Expand Long PCR for fragile X mutation detection (pages 147–154)

      Silva Hećimović, Ingeborg Barišić, Andreas Müller, Iskra Petković, Ivo Barić, Ivo Ligutić and Krešimir Pavelić

      Article first published online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1997.tb02535.x

    4. X-linked severe mental retardation and a progressive neurological disorder in a Belgian family: clinical and genetic studies (pages 155–161)

      Stephan Claes, Koenraad Devriendt, Patrizia D'Adamo, Jan Meireleire, Peter Raeymaekers, Daniela Toniolo, Jean-Jacques Cassiman and Jean-Pierre Fryns

      Article first published online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1997.tb02536.x

    5. Differences in the prevalence of a TaqI RFLP in the 3‘ flanking region of the α1-proteinase inhibitor gene between asthmatic and non-asthmatic black and white South Africans (pages 162–166)

      Samantha L. Green, M. Christine Gaillard, John B. Dewar, Herbert Ludewick, Ernest Song and Charles Feldman

      Article first published online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1997.tb02537.x

    6. Influence of APOH protein polymorphism on apoH levels in normal and diabetic subjects (pages 167–172)

      Gianluca Ruiu, Roberto Gambino, Fabrizio Veglia, Gianfranco Pagano and Maurizio Cassader

      Article first published online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1997.tb02538.x

  2. Case Report

    1. Top of page
    2. Original Article
    3. Case Report
    4. Short Communication
    5. Short Report on DNA Marker at Candidate Locus
    6. Letter to the Editor
    1. A case of de novo interstitial deletion of chromosome 5(q33q34) (pages 173–176)

      Jacques C. Giltay, Klasien B. J. Gerssen-Schoorl, Gert H. J. Luitse and Hans G. Dauwerse

      Article first published online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1997.tb02539.x

    2. Rhombencephalosynapsis with facial anomalies and probable autosomal recessive inheritance: a case report (pages 184–186)

      Marta Romanengo, Paolo Tortori-Donati and Maja Di Rocco

      Article first published online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1997.tb02542.x

  3. Short Communication

    1. Top of page
    2. Original Article
    3. Case Report
    4. Short Communication
    5. Short Report on DNA Marker at Candidate Locus
    6. Letter to the Editor
    1. Turner syndrome in a mother and daughter: r(X) and fertility (pages 187–191)

      Andrea L. Blumenthal and Judith E. Allanson

      Article first published online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1997.tb02543.x

  4. Short Report on DNA Marker at Candidate Locus

    1. Top of page
    2. Original Article
    3. Case Report
    4. Short Communication
    5. Short Report on DNA Marker at Candidate Locus
    6. Letter to the Editor
    1. Intragenic tetranucleotide repeat polymorphism at the human histidase (HAL) locus (pages 194–195)

      Piermario Maffei, Maria Nobile, Daniela Di Bella, Emanuela Novelli, Enrico Smeraldi and Marco Catalano

      Article first published online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1997.tb02545.x

  5. Letter to the Editor

    1. Top of page
    2. Original Article
    3. Case Report
    4. Short Communication
    5. Short Report on DNA Marker at Candidate Locus
    6. Letter to the Editor
    1. Recurrent omphalocele with partial trisomy 3q and partial monosomy 11q (pages 196–198)

      Chih-Ping Chen, Chen-Chi Lee, Chun-Yu Chiang, Dai-Dyi Town, Meng-Shan Lee and Ming-Hong Chen

      Article first published online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1997.tb02546.x

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