Clinical Genetics

Cover image for Clinical Genetics

December 1990

Volume 38, Issue 6

Pages 401–479

  1. Original Article

    1. Top of page
    2. Original Article
    3. Case Report
    4. Announcements
    1. Association of DNA-haplotypes in the human LDL-receptor gene with normal serum cholesterol levels (pages 401–409)

      H. Schuster, S. Humphries, G. Rauh, C. Held, Ch. Keller, G. Wolfram and N. Zöllner

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1990.tb03604.x

    2. Excess of HLA parental sharing in families with Turner patients (pages 415–421)

      M. Cuccia, M. Martinetti, D. Larizza, P. F. Bolis and F. Severi

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1990.tb03606.x

    3. Exclusion mapping of the Cohen syndrome gene from the Prader-Willi syndrome locus (pages 422–426)

      Ikuko Kondo, Jun-ichi Hamabe, Kohtaro Yamamoto and Norio Niikawa

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1990.tb03607.x

    4. Homozygous C4A deficiency in systemic lupus erythematosus: analysis of patients from a defined population (pages 427–433)

      G. Sturfelt, L. Truedsson, P. Johansen, H. Jonsson, O. Nived and A. G. Sjöholm

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1990.tb03608.x

    5. Common intragenic and extragenic polymorphisms of blood coagulation factors VIII and IX are different in Chinese and Caucasian populations (pages 434–440)

      Corinne de la Salle, Qingyu Wu, Marie-Jeanne Baas, André Hanauer, Changgeng Ruan and Jean-Pierre Cazenave

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1990.tb03609.x

    6. Craniofrontonasal dysostosis: variable expression in a three-generation family (pages 441–446)

      Juha Kere, Annukka Ritvanen, Eino Marttinen and Ilkka Kaitila

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1990.tb03610.x

    7. Emery-Dreifuss syndrome in three generations of females, including identical twins (pages 447–451)

      Karen Helene Ørstavik, Reidar Kloster, Carl Lippestad, Lars Rode, Torstein Hovig and Kari Nissen Fuglseth

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1990.tb03611.x

    8. Clinical expression of Menkes syndrome in females (pages 452–459)

      A.-M. Gerdes, T. Tønnesen, N. Horn, T. Grisar, W. Marg, A. Müller, R. Reinsch, N. W. Barton, P. Guiraud, A. Joannard, M. J. Richard and F. Güttler

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1990.tb03612.x

    9. Attitudes of parents of cystic fibrosis children towards neonatal screening and antenatal diagnosis (pages 460–465)

      L. N. Al-Jader, M. C. Goodchild, H. C. Ryley and P. S. Harper

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1990.tb03613.x

  2. Case Report

    1. Top of page
    2. Original Article
    3. Case Report
    4. Announcements
    1. Re-evaluation of GM2346 from a del(16)(q22) to t(4;16)(q35;q22.1) (pages 466–468)

      D. F. Callen, E. G. Baker and S. A. Lane

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1990.tb03614.x

    2. Diagnosis of familial amyloidotic polyneuropathy in France (pages 469–473)

      F. Satier, W. C. Nichols and M. D. Benson

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1990.tb03615.x

    3. An isolated case of Duchenne muscular dystrophy (DMD) in a female with a deletion of DMD cDNA (pages 474–478)

      Mieko Yoshioka, Yoshihiro Yamamoto and Jun-ichi Furuyama

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1990.tb03616.x

  3. Announcements

    1. Top of page
    2. Original Article
    3. Case Report
    4. Announcements
    1. Announcements (page 479)

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1990.tb03617.x

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