1. C-band polymorphisms of chromosome 9: quantification by C_e-bands

   • Kristine Wahedi
   • Ivar Harry Pawlowitzki

   Original Investigations Pages: 1 - 5

2. Steroid sulphatase levels are higher in males than in females of the root vole (Microtus oeconomus)

   • Ulf H. Wiberg
   • Karl Fredga

   Original Investigations Pages: 6 - 11

3. Genesis and systematization of cardiovascular anomalies and analysis of skeletal malformations in murine trisomy 16 and 19

   • C. Bacchus
   • H. Sterz
   • H. Winking

   Original Investigations Pages: 12 - 22

4. An interstitial duplication of the X chromosome in a male allows physical fine mapping of probes from the Xq13-q22 region

   • F. P. M. Cremers
   • R. A. Pfeiffer
   • H. H. Ropers

   Original Investigations Pages: 23 - 27

5. Antioxidant status of Fanconi anemia fibroblasts

   • Johan J. P. Gille
   • Heleen M. Wortelboer
   • Hans Joenje

   Original Investigations Pages: 28 - 31

6. Familial hypercholesterolemia in South African Afrikaners

   • P. A. Brink
   • L. T. Steyn
   • D. R. Van der Westhuyzen

   Original Investigations Pages: 32 - 35

7. Lack of association and linkage between HLA and familial polyposis coli

   • Masayuki Sasaki
   • Kenji Sugio
   • Takehiko Sasazuki

   Original Investigations Pages: 36 - 39

8. Characterization of chromosomes with hybrid genes for Hb Lepore-Washington, Hb Lepore-Baltimore, Hb P-Nilotic, and Hb Kenya

   • K. D. Lanclos
   • J. Patterson
   • T. H. J. Huisman

   Original Investigations Pages: 40 - 45

9. p82H identifies sequences at every human centromere

   • Carmen Aleixandre
   • Dorothy A. Miller
   • Orlando J. Miller

   Original Investigations Pages: 46 - 50

10. De novo complex autosomal translocation involving chromosomes 8, 13 and 15 in a girl with a sporadic retinoblastoma

    • E. Calzolari
    • P. Palazzi
    • F. Bernardi

    Original Investigations Pages: 51 - 54

11. Genetic hemochromatosis and HLA linkage

    • Lawrie W. Powell
    • Janez Ferluga
    • Sue Serjeantson

    Original Investigations Pages: 55 - 56

12. The human inactivated X chromosome folds in early metaphase, prometaphase, and prophase

    • Daniel L. Van Dyke
    • Maria J. Worsham
    • Lester Weiss

    Original Investigations Pages: 57 - 59

13. Multipoint genetic mapping of the Xq26-q28 region in families with fragile X mental retardation and in normal families reveals tight linkage of markers in q26–q27

    • I. Oberlé
    • G. Camerino
    • J. L. Mandel

    Original Investigations Pages: 60 - 65

14. Diagnosis of genetic disease using recombinant DNA. Supplement

    • David N. Cooper
    • Jörg Schmidtke

    Original Investigations Pages: 66 - 75

15. PGI*3(Israel), a new, unstable allele in the phosphoglucose isomerase system

    • B. Bonné-Tamir
    • S. S. Papiha
    • B. Ramot

    Original Investigations Pages: 76 - 79

16. Congenital thyroxine binding globulin deficiency: incidence and inheritance

    • Malcolm B. Jenkins
    • Michael W. Steffes

    Original Investigations Pages: 80 - 84

17. Prevalence of the fragile X syndrome in four birth cohorts of children of school age

    • M. Kähkönen
    • T. Alitalo
    • J. Leisti

    Short Communications Pages: 85 - 87

18. A small deletion in the Duchenne/Becker muscular dystrophy locus —a functionally important region?

    • K. A. Hart
    • A. P. Monaco
    • M. Bobrow

    Short Communications Pages: 88 - 91

19. A fragile X female with Down syndrome

    • T. Arinami
    • I. Kondo
    • T. Hirano

    Clinical Case Report Pages: 92 - 94