Clinical Genetics

Cover image for Clinical Genetics

February 1977

Volume 11, Issue 2

Pages 83–241

  1. Original Article

    1. Top of page
    2. Original Article
    3. Announcement
    1. Cystic fibrosis: Evidence for a genetic compound from a family study in cell culture (pages 83–90)

      B. Shannon Danes, Margaret E. Hodson and J. Batten

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1977.tb01284.x

    2. Two XX males in one family and additional observations bearing on the etiology of XX males (pages 91–106)

      Albert de la Chapelle, Jim Schröder, Juhani Murros and Gustav Tallqvist

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1977.tb01285.x

    3. Morphology of the placenta in fetal I-cell disease (pages 107–113)

      Juhani Rapola and Pertti Aula

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1977.tb01286.x

    4. Adrenoleukodystrophy (Siemerling-Creutzfeldt disease): Heterozygote with two clonal fibroblast populations (pages 114–118)

      H.-H. Ropers, J. Zimmermann and T. Wienker

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1977.tb01287.x

    5. Down syndrome due to partial trisomy 21q (pages 119–121)

      Jaroslav Cervenka, Robert J. Gorlin and Gholman Reza Djavadi

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1977.tb01288.x

    6. 46, X,X-X terminal rearrangement /45, X mosaicism in a child with short stature (pages 122–127)

      D. M. O. Becroft, J. M. Costello and R. L. Shaw

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1977.tb01289.x

    7. X-linked skeletal dysplasia with mental retardation (pages 128–136)

      Joe C. Christian, W. DeMyer, E. A. Franken, J. S. Huff, S. Khairi and T. Reed

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1977.tb01290.x

    8. Heterozygote detection in phenylketonuria (pages 137–146)

      Flemming Güttler and Gert Hansen

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1977.tb01291.x

    9. A case of double trisomy in a liveborn infant: 48, XXY, + 13 (pages 147–150)

      John B. Mailhes, Charleen M. Moore and Juan J. Gershanik

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1977.tb01292.x

    10. Menkes Kinky Hair Syndrome: Is it a treatable disorder? (pages 154–161)

      A. D. Garnica, J. L. Frias and O. M. Rennert

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1977.tb01294.x

    11. Familial occurrence of histiocytosis (pages 163–170)

      E. Frisell, B. Björkstén, G. Holmgren and T. ÅNgström

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1977.tb01295.x

    12. Ganglioside GM2 N-acetyl-ß-D-gafactosaminidase and asialo GM2 (GA2) N-acetyl-ß-D-galactosaminidase; studies in human skin fibroblasts (pages 171–183)

      John S. O'Brien, Anthony G. W. Norden, Arnold L. Miller, Russel G. Frost and Thaddeus E. Kelly

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1977.tb01296.x

    13. A case report of a presumptive +i(18p) associated with serum IgA deficiency (pages 184–188)

      Kohei Ogata, Kazuso Iinuma, Kikuro Kamimura, Ryoko Morinaga and Junko Kato

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1977.tb01297.x

    14. The distribution of ancestral secondary cases in Parkinson's disease (pages 189–192)

      William I. Young, William E. Martin and V. Elving Anderson

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1977.tb01298.x

    15. Genetic heterogeneity of hypoxanthine-phosphoribosyl transferase in human fibroblasts of 3 families (pages 193–200)

      I. Willers, K. R. Held, S. Singh and H. W. Goedde

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1977.tb01299.x

    16. 46,XY, t(3;22)(p2;q13) resuIting in partial trisomy for the short arm of chromosome 3 (pages 201–206)

      Rawatmal B. Surana, Michael E. Braudo, Patrick E. Conen and Reginald H. Slade

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1977.tb01300.x

    17. Partial trisomies of chromosome 21 in man. Two new observations due to translocations 19;21 and 4;21 (pages 207–213)

      Rudolf A. Pfeiffer, Erika K. Kessel and Karl-Heinz Soer

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1977.tb01301.x

    18. Dermatoglyphics in Cri du Chat syndrome (pages 214–218)

      Hiroshi Shiono, Jun-Ichi Kadowaki and Hisashi Kazama

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1977.tb01302.x

    19. The 9p- deletion syndrome A patient with a 45,XX,-9,-15, + t(9/15) constitution due to maternal 3:l meiotic disjunction (pages 219–223)

      F. Bergamo, F. Crosato, D. Francesconi, F. Pasquali and Orsetta Zuffardi

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1977.tb01303.x

    20. Heritability of “sinking” pre-beta lipoprotein level: a twin study (pages 224–226)

      David Hewitt, Jean Milner, Carl Breckenridge and Graham Maguire

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1977.tb01304.x

    21. Two cases of Down syndrome with unusual de novo translocation (pages 227–234)

      Ram S. Verma, David C. Peakman, Arthur Robinson and Herbert A. Lubs

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1977.tb01305.x

    22. Non-fluorescent Y chromosome in a male infant with Turner's symptoms and XO/XY mosaicism (pages 235–240)

      Christa Fonatsch, Sibylle D. Flatz and R. Freyman

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1977.tb01306.x

  2. Announcement

    1. Top of page
    2. Original Article
    3. Announcement
    1. Announcement (page 241)

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1977.tb01307.x

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