Clinical Genetics

Cover image for Clinical Genetics

August 1993

Volume 44, Issue 2

Pages 57–112

  1. Original Article

    1. Top of page
    2. Original Article
    3. Genetics and Society
    4. Letter to the Editor
    5. DNA Report
    6. Announcements
    1. Parental origin of the supernumerary chromosome in trisomy 18 (pages 57–61)

      Xie Ya-gang, Wendy P. Robinson, Roland Spiegel, Franz Binkert, Urszula Ruefenacht and Albert A. Schinzel

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1993.tb03847.x

    2. Infertility in carriers of two bisatellited marker chromosomes (pages 71–75)

      M. Gentile, F. Susca, N. Resta, A. Stella, A. Cascone and G. Guanti

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1993.tb03849.x

    3. Slipped capital femoral epiphysis associated with Rubinstein-Taybi syndrome (pages 79–81)

      Eugenio Bonioli, Carlo Bellini, Filippo M. Sénès, Antonella Palmieri, Mauro Di Stadio and Giorgio Pinelli

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1993.tb03851.x

    4. Effect of the fragile X anomaly on body proportions estimated by pedigree analysis (pages 82–88)

      Danuta Z. Loesch and Mark L. Sampson

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1993.tb03852.x

    5. Application of molecular and cytogenetic techniques to the detection of a de novo unbalanced t(11q;21q) in a patient previously diagnosed as having monosomy 21 (pages 89–94)

      Birgitte Hertz, Carsten A. Brandt, Michael B. Petersen, Søren Pedersen, Ulrich König, Helle Strømkjær and Peter K. A. Jensen

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1993.tb03853.x

    6. Kaufman oculocerebrofacial syndrome: report of two new cases and further delineation (pages 98–101)

      L. E. Figuera, D. Garcia-Cruz, M. L. Ramirez-Dueñas, V. Rivera-Rables and J. M. Cantù

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1993.tb03855.x

  2. Genetics and Society

    1. Top of page
    2. Original Article
    3. Genetics and Society
    4. Letter to the Editor
    5. DNA Report
    6. Announcements
    1. Prenatal screening for cystic fibrosis: attitudes and responses of participants (pages 102–106)

      Moira Mennie, Mary Compton, Annette Gilfillan, R. A. Axton, W. A. Liston, I. Pullen, Dorothy Whyte and D. J. H. Brock

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1993.tb03856.x

  3. Letter to the Editor

    1. Top of page
    2. Original Article
    3. Genetics and Society
    4. Letter to the Editor
    5. DNA Report
    6. Announcements
    1. Ridge hypoplasia and ridge dissociation: minor physical anomalies in autistic children (pages 107–108)

      Isabel Arrieta, Begoña Martinez, Begoña Criado and Natividad Lobato

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1993.tb03857.x

    2. 46XY/47XYY mosaicism and fragile X (pages 109–110)

      J. Bodurtha, C. Jackson-Cook, A. Maddalena, J. Piserchio and R. Waller

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1993.tb03858.x

  4. DNA Report

    1. Top of page
    2. Original Article
    3. Genetics and Society
    4. Letter to the Editor
    5. DNA Report
    6. Announcements
    1. Mspl RFLP in exon 18 of the LDL receptor gene detectable by PCR (page 111)

      Kari Solberg, Olaug K. Rødningen, Serena Tonstad, Leiv Ose, Kåre Berg and Trond P. Leren

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1993.tb03859.x

  5. Announcements

    1. Top of page
    2. Original Article
    3. Genetics and Society
    4. Letter to the Editor
    5. DNA Report
    6. Announcements
    1. Announcements (page 112)

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1993.tb03860.x

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