Clinical Genetics

Cover image for Clinical Genetics

May 1985

Volume 27, Issue 5

Pages 433–528

  1. Original Article

    1. Top of page
    2. Original Article
    3. Letters to the Editors
    1. Low density lipoprotein receptor activity in cultured skin fibroblasts from octa- and nonagenarians (pages 433–442)

      Trond P. Leren, Kjell Maartmann-Moe and Kåre Berg

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1985.tb00228.x

    2. Glycosphingolipid studies of visceral tissues and brain from type 1 Gaucher disease variants (pages 443–450)

      Olle Nilsson, Gregory A. Grabowski, Mark D. Ludman, Robert J. Desnick and Lars Svennerholm

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1985.tb00229.x

    3. Chromosome analysis in 100 cases of first trimester trophoblast sampling (pages 451–457)

      Sverre Heim, Ulf Kristoffersson, Nils Mandahl, Anita Mineur, Felix Mitelman, Helene Edvall and Björn Gustavii2

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1985.tb00230.x

    4. Increased frequency of the apolipoprotein E-4 isoform in male subjects with multifactorial hypercholesterolemia (pages 458–462)

      Trond P. Leren, Anne-Lise Bbøresen, Kåre Berg, Ingvar Hjermann and Paul Luren

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1985.tb00231.x

    5. Effect of folic acid treatment in the fragile X syndrome (pages 463–467)

      Karl-Henrik Gustavson, Kate Dahlbom, Anders Flood, Gösta Holmgren, Hans K[RIGHTWARDS ARROW]son Blomquist and Gunnar Sanner

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1985.tb00232.x

    6. X-linked Ehlers-Danlos syndrome type V; the next generation (pages 472–478)

      Peter Beighton and Diana Curtis

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1985.tb00234.x

    7. Prenatal diagnosis of glycogenosis type II (Pompe's disease) using chorionic villi biopsy (pages 479–482)

      Anne-Marie Besançon, Laetitia Castelnau, Henriette Nicolesco, Yves Dumez and Livia Poenaru

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1985.tb00235.x

    8. Consanguinity among the Kuwaiti population (pages 483–486)

      S. A. Al-Awadi, M. A. Moussa, K. K. Naghuib, T. I. Farag, A. S. Teebi, M. El-Khalifa and L. El-Dossary

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1985.tb00236.x

    9. Unbalanced karyotype with normal phenotype in a family with translocation (8;13) (p21;q22) (pages 487–495)

      A. H. J. T. Bröcker-Vriends, J. J. P. van de Kamp, J. P. M. Geraedts, S. E. Bos and Th. A. Nijenhuis

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1985.tb00237.x

    10. Centromeric instability of chromosomes 1 and 16 with variable immune deficiency: a new syndrome (pages 501–505)

      P. J. Howard, I. J. Lewis, F. Harris and S. Walker

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1985.tb00239.x

    11. Gustatory lacrimation in association with the branchio-oto-renal syndrome (pages 506–509)

      James W. Preisch, David Bixler and Forrest D. Ellis

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1985.tb00240.x

    12. A folate sensitive heritable fragile site at 19p13 (pages 510–514)

      Niels Tommerup, Johannes Nielsen and Margareta Mikkelsen1

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1985.tb00241.x

    13. Two cases of interstitial deletion of the long arm of chromosome 1: del(1)(q21 [RIGHTWARDS ARROW] q25) and del(1)(q41 [RIGHTWARDS ARROW] q43) (pages 515–519)

      F. A. Beemer, J. M. Klep-de Pater, G. J. Sepers and B. Janssen

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1985.tb00242.x

  2. Letters to the Editors

    1. Top of page
    2. Original Article
    3. Letters to the Editors
    1. Detection of the fragile X chromosome and other fragile sites (pages 520–521)

      Graham C. Webb

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1985.tb00243.x

    2. Complex glycerol kinase deficiency syndrome explained as X-chromosomal deletion (pages 522–523)

      B. Wieringa, Th. Hustinx, J. Scheres, W. Renier and B. ter Haar

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1985.tb00244.x

    3. Antenatal diagnosis of infantile Refsum's disease (pages 524–526)

      B. T. Poll-The, A. Poulos, P. Sharp, J. Boue, H. Ogier, M. Odièvre and J. M. Saudubray

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1985.tb00246.x

    4. Marker chromosome in cat eye syndrome (pages 526–528)

      Ram S. Verma, K. A. Babu, W. Rosenfeld and R. C. Jhaveri

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1985.tb00247.x

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