Clinical Genetics

Cover image for Clinical Genetics

November 1998

Volume 54, Issue 5

Pages 375–446

  1. Mini Review

    1. Top of page
    2. Mini Review
    3. HotSpots
    4. Original Article
    5. Short Report
    6. Letter to the Editor
    7. Announcements
    1. Genetic testing and insurance in the United Kingdom (pages 375–379)

      PJ Morrison

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1998.tb03749.x

  2. HotSpots

    1. Top of page
    2. Mini Review
    3. HotSpots
    4. Original Article
    5. Short Report
    6. Letter to the Editor
    7. Announcements
    1. HotSpots (pages 380–384)

      M. E. Suzanne Lewis

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1998.tb03750.x

  3. Original Article

    1. Top of page
    2. Mini Review
    3. HotSpots
    4. Original Article
    5. Short Report
    6. Letter to the Editor
    7. Announcements
    1. Genetic variation in paraoxonase-2 is associated with variation in plasma lipoproteins in Canadian Oji-Cree (pages 394–399)

      Robert A Hegele, Stewart B Harris, Philip W Connelly, Anthony JG Hanley, Lap-Chee Tsui, Bernard Zinman and Stephen W Scherer

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1998.tb03752.x

    2. Severe malformations in males from families with osteopathia striata with cranial sclerosis (pages 400–405)

      AL Bueno, FJ Ramos, O. Bueno, JL Olivares, ML Bello and M. Bueno

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1998.tb03753.x

  4. Short Report

    1. Top of page
    2. Mini Review
    3. HotSpots
    4. Original Article
    5. Short Report
    6. Letter to the Editor
    7. Announcements
    1. Molecularly proven hypochondroplasia with cloverleaf skull deformity: a novel association (pages 417–420)

      Brad Angle, Joseph H Hersh and Katherine M Christensen

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1998.tb03756.x

    2. Prenatal diagnosis of a trisomy 17p derived from a de novo non-mosaic satellited marker (pages 421–425)

      Anita S Kulharya, Jaime Garcia-Heras, Heather B Radtke, Karen S Norris, Laura D Keppen and David B Flannery

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1998.tb03757.x

    3. Risk factors for mortality in young children living under various socio-economic conditions in Lahore, Pakistan: with particular reference to inbreeding (pages 426–434)

      Muhammad Yaqoob, Sven Cnattingius, Fehmida Jalil, Shakila Zaman, Lennart Iselius and Karl-Henrik Gustavson

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1998.tb03758.x

  5. Letter to the Editor

    1. Top of page
    2. Mini Review
    3. HotSpots
    4. Original Article
    5. Short Report
    6. Letter to the Editor
    7. Announcements
    1. Detection of more than 91% cystic fibrosis mutations in a sample of the population from Reunion Island and identification of two novel mutations (A309G, S1255L) and one novel polymorphism (L49L) (pages 437–439)

      F. Cwtuult, J. Stefjrrrnn, D. Viduud, S. Botrsquet, F. Lestire, M. Renotiil, N. MeDonell, J. Feingold, C. Belrljord and T. Bienvenu

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1998.tb03760.x

    2. Two brothers with hypospadias, hypertelorism, upper lid coloboma and mixed type hearing loss: a new syndrome (pages 440–442)

      Sevim Bulci, Aycan Kayikcioglu and A Safek Dugli

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1998.tb03761.x

  6. Announcements

    1. Top of page
    2. Mini Review
    3. HotSpots
    4. Original Article
    5. Short Report
    6. Letter to the Editor
    7. Announcements
    1. Announcements (page 446)

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1998.tb03763.x

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