1. The nuclear skeleton and the spatial arrangement of chromosomes in the interphase nucleus of vertebrate somatic cells

   • J. Hubert
   • C. A. Bourgeois

   Review Articles Pages: 1 - 15

2. The evolution of the α- and β-globin gene clusters in human populations

   • A. V. S. Hill
   • J. S. Wainscoat

   Review Articles Pages: 16 - 23

3. Repeated DNA sequences in the distal long arm of the human X chromosome

   • U. Müller
   • U. Tantravahi
   • S. A. Latt

   Original Investigations Pages: 24 - 29

4. Mapping through somatic cell hybrids and cDNA probes of protein C to chromosome 2, factor X to chromosome 13, and α1-acid glycoprotein to chromosome 9

   • M. Rocchi
   • L. Roncuzzi
   • G. Romeo

   Original Investigations Pages: 30 - 33

5. Regional assignment of human liver-type 6-phosphofructokinase to chromosome 21q22.3 by using somatic cell hybrids and a monoclonal anti-L antibody

   • Margaret Van Keuren
   • H. Drabkin
   • Shobhana Vora

   Original Investigations Pages: 34 - 40

6. Ehlers-Danlos syndrome type IV: cosegregation of the phenotype to a COL3A1 allele of type III procollagen

   • P. Tsipouras
   • P. H. Byers
   • F. Ramirez

   Original Investigations Pages: 41 - 46

7. Osteogenesis imperfecta type IV: evidence of abnormal triple helical structure of type I collagen

   • R. J. Wenstrup
   • A. G. W. Hunter
   • P. H. Byers

   Original Investigations Pages: 47 - 53

8. Hemoglobin abnormalities

   • M. Lallemant
   • F. Galacteros
   • J. Rosa

   Original Investigations Pages: 54 - 58

9. Attenuated activities and structural alterations of arylsulfatase A in tissues from subjects with pseudo arylsulfatase A deficiency

   • H. Kihara
   • W. E. Meek
   • A. L. Fluharty

   Original Investigations Pages: 59 - 62

10. Location of the X inactivation center in primates and other mammals

    • Wendy L. Flejter
    • D. L. Van Dyke
    • L. Weiss

    Original Investigations Pages: 63 - 66

11. The fragile site (16) (q22)

    • M. Schmid
    • W. Feichtinger
    • R. Lange

    Original Investigations Pages: 67 - 73

12. The myoblast defect identified in Duchenne muscular dystrophy is not a primary expression of the DMD mutation

    • Cecelia Webster
    • G. Filippi
    • Helen M. Blau

    Original Investigations Pages: 74 - 80

13. Cytogenetic effects of methyl isocyanate exposure in Bhopal

    • H. K. Goswami

    Original Investigations Pages: 81 - 84

14. Different inducibility and possible significance of several concomitant “fragile sites” in two brothers

    • F. Shabtai
    • J. Orlin
    • J. Friedman

    Original Investigations Pages: 85 - 89

15. A Taq1 γ-globin DNA polymorphism: an African-specific marker

    • J. S. Wainscoat
    • A. E. Kulozik
    • D. J. Weatherall

    Original Investigations Pages: 90 - 92

16. Analysis of linkage relationships between genetic markers around the fragile X locus with special reference to the daughters of normal transmitting males

    • R. M. Winter
    • M. E. Pembrey

    Original Investigations Pages: 93 - 97

17. Fluctuation of a clone 46,XX,i(7q) in bone marrow in a Fanconi anaemia

    • J. L. Huret
    • Elisabeth Benz
    • J. Tanzer

    Short Communications Pages: 98 - 100

18. Human chromosome hot points

    • Ning Li
    • Ye Wu
    • Xianting Zhou

    Short Communications Pages: 101 - 103

19. Polysomy of chromosome 7 is correlated with overexpression of the erbB oncogene in human glioblastoma cell lines

    • W. Henn
    • N. Blin
    • K. D. Zang

    Short Communications Pages: 104 - 106