1. Dyslexia revisited

   • M. Herschel

   Review Articles Pages: 115 - 134

2. Double translocation t(7;12),t(2;6) heterozygosity in one family

   • Jan B. Bijlsma
   • Henny F. de France
   • Piet F. Dijkstra

   Original Investigations Pages: 135 - 147

3. Quantitative studies on the arrangement of human metaphase chromosomes

   • H. Zankl
   • K. D. Zang

   Original Investigations Pages: 149 - 155

4. A new variety of spondyloepiphyseal dysplasia characterized by punctate corneal dystrophy and abnormal dermal collagen fibrils

   • Peter H. Byers
   • Karen A. Holbrook
   • John W. Chandler

   Original Investigations Pages: 157 - 169

5. Quinacrine and acridine-R banding without a fluorescence microscope

   • Y. Nakagome
   • S. Oka
   • M. Higurashi

   Original Investigations Pages: 171 - 176

6. Heterogeneity of glucose-6-phosphate dehydrogenase deficiency in Algeria

   • M. Benabadji
   • F. Merad
   • J. C. Kaplan

   Original Investigations Pages: 177 - 184

7. Effect of phospholipases on Factor-VIII activity

   • R. Ananthakrishnan
   • S. D'Souza

   Original Investigations Pages: 185 - 191

8. Effects of caffeine on sister chromatid exchange (SCE) after exposure to UV light or triaziquone studied with a fluorescence plus Giemsa (FPG) technique

   • W. Vogel
   • Th. Bauknecht

   Original Investigations Pages: 193 - 198

9. Silver-staining specificity in metaphases after incorporation of 5-bromodeoxyuridine (BUDR)

   • W. Vogel
   • W. Schempp
   • V. Puel

   Original Investigations Pages: 199 - 203

10. Differential silver carbonate staining of sister chromatids in BrdU-substituted chromosomes

    • V. J. Goyanes

    Short Communications Pages: 205 - 208

11. Monogene inheritance of learning speed in DBA and C3H mice

    • W. Buselmaier
    • S. Geiger
    • W. Reichert

    Short Communications Pages: 209 - 214

12. Human liver alcohol dehydrogenase isoenzyme variations

    • Shoji Harada
    • Dharam P. Agarwal
    • H. Werner Goedde

    Short Communications Pages: 215 - 220

13. Successive spontaneous abortions including one with whole-arm translocation between chromosomes 2

    • Koso Ohama
    • Ichiro Kusumi
    • Tadashi Kajii

    Clinical Case Reports Pages: 221 - 225

14. Isochromosome for the long arm of the Y in an infertile male

    • Mark C. Taylor
    • H. Allen Gardner
    • C. Ezrin

    Clinical Case Reports Pages: 227 - 230

15. Autosomal recessive sensorineural-conductive deafness, mental retardation, and pinna anomalies

    • J. M. Cantú
    • R. Ruenes
    • D. Garcia-Cruz

    Clinical Case Reports Pages: 231 - 234

16. Models and assumptions in calculating the probabilities of detecting chromosomal mosaicism

    • Ernest B. Hook

    Letters to the Editors Pages: 235 - 239

17. Announcement

    Announcement Pages: i - i