Clinical Genetics

© John Wiley & Sons A/S

Cover image for Clinical Genetics

November 1987

Volume 32, Issue 5

Pages 289–367

  1. Original Article

    1. Top of page
    2. Original Article
    1. Linkage of G8 (D4S10) in two Swedish families with Huntington's disease (pages 289–294)

      G. Holmgren, E. Winnberg Almqvtst, M. Anyret, M. Conneally, W. Hobbs, B. Mattsson, J. Wahlström, B. Winblad and J. F. Gusella

      Article first published online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1987.tb03292.x

    2. Prader-Willi syndrome in two siblings: one with normal karyotype, one with a terminal deletion of distal Xq (pages 295–299)

      Tatsuya Ishikawa, Manabu Kanayama and Yoshiro Wada

      Article first published online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1987.tb03293.x

    3. Homozygous variegate porphyria A severe skin disease of Infancy (pages 300–305)

      Pertti Mustajoki, Raimo Tenhunen, Kirsti Maria Niemi, Yves Nordmann, Helena Kääriäinen and Reijo Norio

      Article first published online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1987.tb03294.x

    4. New type of spinocerebellar degeneration syndrome in a northern Swedish population (pages 306–312)

      K.-H. Gustavson, K. Modrzewska, A. Erikson and U. Andersson

      Article first published online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1987.tb03295.x

    5. Progressive mental regression in siblings with Morquio disease Type B (mucopolysaccharidosis IV B) (pages 313–325)

      R. Giuguani, M. Jackson, S. J. Skinner, C. M. Vimal, A. H. Fensom, N. Fahmy, A. Sjövall and P. F. Benson

      Article first published online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1987.tb03296.x

    6. X-linked dysmorphic syndrome with mental retardation (pages 326–334)

      F. Prieto, L. Badía, F. Mulas, A. Monfort and F. Mora

      Article first published online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1987.tb03297.x

    7. Familial dysbetalipoproteinemic subjects with the E3/E2 phenotype exhibit an E2 isoform with only one cysteine residue (pages 335–341)

      Maruke Smit, Peter de Knuff, Rune R. Frants, Eduard C. Klasen and Louis M. Havekes

      Article first published online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1987.tb03298.x

    8. Free proximal trisomy 21 without the Down syndrome (pages 342–348)

      Jonathan P. Park, Doris H. Wurster-Hill, Patricia A. Andrews, William C. Cooley and John M. Graham

      Article first published online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1987.tb03299.x

    9. A rapid and efficient screening method for DNA restriction fragment length polymorphisms (pages 349–354)

      Thomas L. J. Boehm, Andreas Werle and Dusan Drahovsky

      Article first published online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1987.tb03300.x

    10. A new autosomal dominant craniofacial deafness syndrome (pages 355–359)

      S. Kassutto, Z. Kassutto, T. Ben-Ami and R. M. Goodman

      Article first published online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1987.tb03301.x

    11. X-linked muscular dystrophy with early contractures and cardiomyopathy (Emery-Dreifuss type) (pages 360–367)

      Alan E. H. Emery

      Article first published online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1987.tb03302.x

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