Clinical Genetics

Cover image for Clinical Genetics

November 1979

Volume 16, Issue 5

Pages 297–368

  1. Original Article

    1. Top of page
    2. Original Article
    1. Genetic basis of acquired C4 deficiency (pages 297–300)

      J. J. Cream, B. Olaisen, P. Teisberg, A. V. Soler and R. A. Thompson

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1979.tb01005.x

    2. An autosomal dominantly inherited syndrome of facial asymmetry, esotropia, amblyopia, and submucous cleft palate (Bencze syndrome) (pages 301–304)

      David Kurnit1, Judith G. Hall, David B. Shurtleff and M. Michael Cohen Jr.

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1979.tb01006.x

    3. Phenotypic variation in two patients with a ring chromosome 22 (pages 305–310)

      S. J. FUNDERBURK, R. S. SPARKES and I. KLISAK

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1979.tb01007.x

    4. Lumbar kyphosis in Hunter's disease (MPS II) (pages 317–322)

      P. F. Benson, L. R. Button, A. H. Fensom and M. F. Dean

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1979.tb01009.x

    5. Neuraminidase deficiency in the original patient with the Goldberg Syndrome (pages 323–330)

      George H. Thomas, Morton F. Goldberg, Carol S. Miller and Linda W. Reynolds

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1979.tb01010.x

    6. A distinct variant of the Ehlers-Danlos syndrome (pages 335–339)

      A. Hernández, M. G. Aguirre-Negrete, S. Ramírez-Soltero, A. González-Mendoza, R. MartínezY Martínez, A. Velázquez-Cabrera and J. M. Cantú

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1979.tb01012.x

    7. Interstitial deletion 13q33 resulting from maternal insertional translocation (pages 340–346)

      B. S. Emanuel, E. H. Zackai, L. Moreau, P. Coates and E. Orrechio

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1979.tb01013.x

    8. Heterozygote detection in glucose-6-phosphate dehydrogenase deficiency: limitation of hair follicle analysis (pages 353–356)

      A. J. M. Vermorken, G. Th. Spierenburg, C. A. van Bennekom, C. H. M. M. de Bruyn, T. L. Oei, G. E. J. Staal and R. A. Geerdink

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1979.tb01015.x

    9. Human amniotic fluid CX-L-fucosidase (pages 357–363)

      Jack A. Alhadeff and Grai L. Andrews-Smtth

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1979.tb01016.x

    10. Fanconi's anaemia associated with haemophilia A (pages 364–368)

      Rolf Ljung, Lars Holmberg, Karl-Olof Nilsson and Astrid Thilén

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1979.tb01017.x

SEARCH

SEARCH BY CITATION