Clinical Genetics

Cover image for Clinical Genetics

January 1995

Volume 47, Issue 1

Pages 1–56

  1. Original Article

    1. Top of page
    2. Original Article
    3. Case Report
    4. Announcements
    1. Plasma lipids and lipoproteins response to a dietary challenge: analysis of four candidate genes (pages 1–12)

      Yechiel Friedlander, Elliot M. Berry, Shlomo Eisenberg, Yechezkiel Stein and Eran Leitersdorf

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1995.tb03913.x

    2. Risk estimates for developing motor neurone disease in first-degree relatives (pages 13–16)

      C. M. James, R. G. Newcombe, P. S. Harper and C. M. Wiles

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1995.tb03914.x

    3. Maternal 3;13 chromosome insertion, with severe pre-eclampsia (pages 17–21)

      P. A. Boyd, E. J. Maher, R. H. Lindenbaum, A. M. Hoogwerf, C. Redman and M. Crocker

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1995.tb03915.x

    4. Increased frequency of the rare PstI allele (P2) in a population of CAD patients in Northern Greece (pages 22–26)

      Norma A. Vavatsi, Sophia A. Kouidou, Paraschos N. Geleris, Christos Tachmatzidis, Theodoros Gikas, Demetrios K. Tsifodimos and Antonios C. Trakatellis

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1995.tb03916.x

    5. Charcot-Marie-Tooth disease: molecular characterization of patients from Central and Southern Italy (pages 27–32)

      V. Guzzetta, L. Santoro, P. Gasparo-Rippa, M. Ragno, G. Vita, G. Caruso and G. Andria

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1995.tb03917.x

    6. Familial microcephaly with severe neurological deficits: a description of five affected siblings (pages 33–37)

      V. Gross-Tsur, A. Joseph, G. Blinder and N. Amir

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1995.tb03918.x

    7. Dicentric chromosome Y associated with Leydig cell agenesis and sex reversal (pages 38–41)

      Maurizio Genuardi, Barbara Bardoni, Giovanna Floridia, Pietro Chiurazzi, Gioacchino Scarano, Marcella Zollino, Nicola Garcea, Maria Enrica Martini-Neri and Giovanni Neri

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1995.tb03919.x

    8. Factors influencing whether or not couples seek genetic counselling: an explorative study in a paediatric surgical unit (pages 47–52)

      Inge Hobus, Petra G. Frets, Hugo J. Duivenvoorden, Dick Tibboel and Martinus F. Niermeijer

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1995.tb03921.x

  2. Case Report

    1. Top of page
    2. Original Article
    3. Case Report
    4. Announcements
    1. Antley-Bixler syndrome and esophageal atresia in a patient with trisomy 21 (pages 53–55)

      E. Feigin, R. Udassin, D. Seror, A. Szold, Z. Ben Neriah and B. Glick

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1995.tb03922.x

  3. Announcements

    1. Top of page
    2. Original Article
    3. Case Report
    4. Announcements
    1. Announcements (page 56)

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1995.tb03923.x

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