Clinical Genetics

Cover image for Clinical Genetics

February 1992

Volume 41, Issue 2

Pages 57–111

  1. Original Article

    1. Top of page
    2. Original Article
    3. Announcements
    1. Autosomal recessive blepharophimosis, ptosis, V-esotropia, syndactyly and short stature (pages 57–61)

      M. Frydman, H. A. Cohen, G. Karmon and H. Savir

      Article first published online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1992.tb03632.x

    2. The thymic findings in stillborns with neural tube defects (pages 62–64)

      Fatma Nur Seniz

      Article first published online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1992.tb03633.x

    3. Autosomal dominant congenital cataract; linkage relations; clinical and genetic heterogeneity (pages 65–69)

      Allan M. Lund, Hans Eiberg, Thomas Rosenberg and Mette Warburg

      Article first published online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1992.tb03634.x

    4. Familial amyloidotic polyneuropathy: a new transthyretin position 30 mutation (alanine for valine) in a family of German descent (pages 70–73)

      L. A. Jones, J. C. Skara, A. S. Cohen, J. A. Harding, A. Milunsky and M. Skinner

      Article first published online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1992.tb03635.x

    5. A lethal syndrome resembling branchio-oculo facial syndrome (pages 74–78)

      A. V. Hind, Richard Torack and S. B. Dowton

      Article first published online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1992.tb03636.x

    6. A new form of X-linked, high-frequency, sensorineural deafness (pages 79–81)

      Diana Wellesley and Jack Goldblatt

      Article first published online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1992.tb03637.x

    7. The interstitial deletion of bands q33–35 of long arm of chromosome 7: a review with a new case report (pages 82–86)

      Ram S. Verma, Robert A. Conte, Sami L. Sayegh and Debasis Kanjilal

      Article first published online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1992.tb03638.x

    8. Oculocerebral syndrome with hypopigmentation (Cross syndrome): report of a new case (pages 87–89)

      M. Lerone, A. Possagno, A. Taccone, G. Poggi, G. Romeo and M. C. Silengo

      Article first published online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1992.tb03639.x

    9. A girl with 71,XXXXY karyotype (pages 96–99)

      P. D. Maaswinksl-Mooij, P. van Zwieten, P. Mollevanger, E. van Noort and G. Beverstock

      Article first published online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1992.tb03641.x

    10. Quality control in routine chromosome analysis: prediction of total number of bands for the individual case analyzed (pages 100–104)

      U. Claussan, W. Kleider, H.-G. Muller, N. Wills and H. A. Baumann

      Article first published online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1992.tb03642.x

    11. A boy with Poland anomaly and facio-auriculo-vertebral dysplasia (pages 105–107)

      J. M. Cobben, A. J. van Essen, P. G. McParland, H. A. Polman and L. P. ten Kate

      Article first published online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1992.tb03643.x

    12. Hereditary motor and sensory neuropathy type I, associated with aplasia cutis congenital possible X-linked inheritance (pages 108–110)

      David Castle, Hyam Isaacs, Michale Ramsay and Renee Bernstein

      Article first published online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1992.tb03644.x

  2. Announcements

    1. Top of page
    2. Original Article
    3. Announcements
    1. Announcements (page 111)

      Article first published online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1992.tb03645.x

SEARCH

SEARCH BY CITATION