Clinical Genetics

Cover image for Clinical Genetics

May 1986

Volume 29, Issue 5

Pages 349–476

  1. Original Article

    1. Top of page
    2. Original Article
    3. Letters to the Editors
    4. Fourth Nordic Conference
    1. Indication against genetic localisation of the human transcobalamin II gene (TC2) on chromosome 16 (pages 349–353)

      Martin Gallmann, Marijke Fráter-Schröder, Wolfgang Scheffrahn, Jürg Ott, Balthasar Schmid, Esther Butler, Vreni Biedermann and Lucja Kierat

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb00503.x

    2. Linkage of transcobalamin II (TC2) to the P blood group system and assignment to chromosome 22 (pages 354–359)

      H. Eiberg, N. Møller, J. Mohr and L. S. Nielsen

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb00504.x

    3. Evaluation of urinary cells in acid cholesteryl ester hydrolase deficiency (pages 360–368)

      Subroto Chatterjee, Elisabeth Castiglione, Peter O. Kwiterovich, Jeffrey M. Hoeg and H. Bryan Brewer

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb00505.x

    4. Unspecific reactions of HLA-B antisera on fibroblasts from patients and carriers of Duchenne muscular dystrophy (pages 369–373)

      E. D. Aragon de Kirbach, I. Willers, S. Singh and H. W. Goedde

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb00506.x

    5. Linkage between the loci for cystic fibrosis and paraoxonase (pages 374–377)

      K. Schmiegelow, H. Eiberg, L. -C. Tsui, M. Buchwald, P. D. Phelan, R. Williamson, W. Warwick, E. Niebuhr, J. Mohr, M. Schwartz and C. Koch

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb00507.x

    6. Prometaphase chromosome analysis as a routine diagnostic technique (pages 378–383)

      Islay C. S. Barnes and Edna L. Maltby

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb00508.x

    7. The effect of consanguineous marriages on reproductive wastage (pages 384–388)

      S. A. Al-Awadi, K. K. Naguib, M. A. Moussa, T. I. Farag, A. S. Teebi and M. Y. El-Khalifa

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb00509.x

    8. Genetic screening for artificial insemination by donor (AID) : Results of a study on 676 semen donors (pages 389–396)

      J. Selva, C. Leonard, M. Albert, J. Auger and G. David

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb00510.x

    9. Fetal mortality in sibships of cases with neural tube defects (pages 409–412)

      A. D. Sadovnick, B. Keena, P. A. Baird and J. G. Hall

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb00512.x

    10. Cryptophthalmos - syndactyly syndrome without cryptophthalmos (pages 413–416)

      R. Koenig and J. Spranger

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb00513.x

    11. Infantile type of sialic acid storage disease with sialuria (pages 417–424)

      E. Paschke, G. Trinkl, W. Erwa, M. Pavelka, I. Mutz and A. Roscher

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb00514.x

    12. Whole-arm t (X;17) (Xp17q;Xq17p) and gonadal dysgenesis : A further exception to the critical region hypothesis (pages 425–428)

      H. Rivera, M. A. Eníuquez-Guerra, A. ROLÓN, M. E. JIMÉNEZ-SÁINZ, L. Núñez-Gonzalez and J. M. Cantú

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb00515.x

    13. Germinal mosaicism in Apert syndrome (pages 429–433)

      Judith E. Allanson

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb00516.x

    14. De novo del(4) (p15.32) with incomplete expression of the Wolf-Hirschhorn syndrome (pages 439–444)

      L. P. Castro-Felix, M. L. RamSrez, S. Valera-Huezo, E. Matute, F. Rivas, H. Rivera, M. Moller and J. M. Cantu

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb00518.x

    15. Use of Y chromosome specific probes to detect low level sex chromosome mosaicism (pages 445–448)

      Umadevi Tantravahi, Diana W. Bianchi, Christine Haley, Margaret M. Destrempes, Alyne T. Ricker, Bruce R. Korf and Samuel A. Latt

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb00519.x

    16. Detection and exclusion of carriers of ornithine transcarbamylase deficiency by RFLP analysis (pages 449–452)

      M. Schwartz, Ernst Christensen, Niels C. Christensen, Flemming Skovby, Kay E. Davies and John M. Old

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb00520.x

  2. Letters to the Editors

    1. Top of page
    2. Original Article
    3. Letters to the Editors
    4. Fourth Nordic Conference
    1. Arthrogryposis and 46,XY, t(1;16) chromosome constitution (pages 453–455)

      Françoise Serville, José Dufau-Casanabe and Daniel Fontan

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb00521.x

    2. Heterozygote expression in Grebe Chondrodysplasia (pages 455–456)

      Diana Curtis

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb00522.x

  3. Fourth Nordic Conference

    1. Top of page
    2. Original Article
    3. Letters to the Editors
    4. Fourth Nordic Conference
    1. DNA probes for linkage analysis of X linked diseases: Localisation of the disease locus for anhidrotic ectodermal dysplasia (page 458)

      L. Bolund, P. Ahrens, H. Albertsen, P. K. A. Jensen, T. A. Kruse and S. Kolvraa

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb00523.x

    2. Mapping status of cystic fibrosis (pages 458–459)

      Hans Eiberg, Kjeld Schmiegelow and Jan Mohr

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb00524.x

    3. A computerised register for Huntington's chorea in Denmark (pages 460–461)

      Kirsten Fenger and S. A. Sørensen

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb00525.x

    4. Studies on fragile X-mental retardation by the use of DNA probes (page 462)

      P. Goonewardena, K. H. Gustavson, G. Holmgren, A. Tolun, J. Chotai, E. Johnsen1 and U. PetterssoN

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb00526.x

    5. Characterization of neoplasia-associated chromosome abnormalities by Southern blot analysis (pages 462–463)

      J. Kere, T. Ruutu and A. de la Chapelle

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb00528.x

    6. 235 cases of prenatal 1st trimester cytogenetic diagnosis based on transabdominal CVS (page 462)

      J. M. Hertz, P. K. A. Jensen and A. J. Therkelsen

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb00527.x

    7. Cystic fibrosis - a search for the basic defect (pages 463–464)

      H. Kollberg, A. Bardon and O. Ceder

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb00529.x

    8. RFLP studies in families with Duchenne muscular dystrophy (pages 464–465)

      Mikael Lindlof, Helena Kaariainen and Albert de la Chapelle

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb00531.x

    9. The prognostic implication of cytogenetic findings in non-Hodgkin lymphomas (page 464)

      Ulf Kristoffersson, Sverre Heim, Nils Mandahl, Felix Mitelman, Håkan Olsson, Jonas Ranstam and Måns ÅKerman

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb00530.x

    10. Early diagnosis of Mb. Recklinghausen (pages 465–466)

      Troels Lyngbye and Lars Haugaard

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb00532.x

    11. Chromosome abnormalities in mesenchymal neoplasms (pages 466–467)

      Nils Mandahl, Sverre Heim, Ulf Kristoffersson, Felix Mitelman and Anders Rydholm

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb00534.x

    12. The most profoundly retarded children in the county of Aarhus II. Etiologic and pathogenetic aspects (page 466)

      TROELS Lyngbye, Gudrun Dahl and Hella Koopmann Kristensen

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb00533.x

    13. Single abnormal cells may be interpreted as pseudomosaicism or mosaicism (pages 467–468)

      Pål Møixer and Eli Ormerod

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb00535.x

    14. Restriction enzyme analysis of human HLA-linked C4-genes in the Finnish population (pages 469–470)

      J. Partanen, L. Peltonen and S. Koskimies

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb00538.x

    15. Genetic effects in offspring of cancer patients (page 469)

      Per Oftedal and John Mulvihill

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb00537.x

    16. Polymorphism of type I collagen genes in the Finnish population (page 470)

      L. Peltonen, H. Ahti, A. Palotie and F. Ramirez

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb00539.x

    17. Linkage studies in choroideremia (pages 471–472)

      Eeva-Marja Sankila, Jussi Kärnä, Henrik Forsius, Aldur Eriksson and Albert de la Chapelle

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb00541.x

    18. Mutagenic effect of amniotic fluid from smoking women at term (page 471)

      G. R. O. Nylander Rivrud, Kare Berg, Diana Anderson, Stephen Blowers and Knut Bjøro

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb00540.x

    19. Clinical use of DNA markers (RFLP) in genetic counselling and prenatal diagnosis of haemophilia A and B (pages 472–473)

      Marianne Schwartz, Elma Scheibel and Nanni Din

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb00542.x

    20. Cockayne syndrome, early-onset type: clinical and cytogenetic findings (pages 473–474)

      M. Somer, L. Rossi and T. Jousi

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb00543.x

    21. High-resolution banding: a study of 85 patients with mental retardation (page 474)

      Carola Tengstrom, Seppo Autio and Ulla Gripenberg

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb00544.x

    22. The fragile X chromosome: prenatal diagnosis (page 475)

      Niels Tommerup

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb00545.x

    23. Effect of genetic factors on the variation in plasma concentration of antithrombin III: A twin study (pages 475–476)

      K. H. Orstavik, P. Magnus, K. Maartmann-Moe and K. Berg

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb00546.x

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