1. Partial monosomies 18

   • I. W. Lurie
   • G. I. Lazjuk

   Reviews Pages: 203 - 222

2. Beobachtungen einer Familie mit Galaktosämie und “Duarte-Variante”

   • Gesine Haschemian
   • Fritz Menne

   Originalarbeiten Pages: 223 - 226

3. Serogenetic investigations on malignant melanomas with reference to the incidence of AB0 system, Rh system, Gm, Inv, Hp and Gc systems

   • G. Jörgensen
   • V. B. Lal

   Original Investigations Pages: 227 - 231

4. Geometric fitness coefficients and inbreeding

   • R. Chakraborty
   • J. K. Ghorai

   Original Investigations Pages: 232 - 235

5. The correspondence between quinacrine banding patterns and sites of secondary constrictions in human chromosomes

   • I. H. Pawlowitzki

   Original Investigations Pages: 236 - 241

6. A newborn with the cat-eye syndrome

   • J. P. Fryns
   • E. Eggermont
   • H. van den Berghe

   Original Investigations Pages: 242 - 248

7. Identification of individual chromosomes in the human karyotype by their banding pattern after proteolytic digestion

   • Catherine Finaz
   • Jean de Grouchy

   Short Communications Pages: 249 - 252

8. Identification of two Robertsonian translocations with a Giemsa banding technique

   • J. M. J. C. Scheres

   Short Communications Pages: 253 - 256

9. Incidence of cardiac malformations in Greenlandic Eskimos

   • B. Harvald
   • J. Hels

   Short Communications Pages: 257 - 260

10. Ultrastructural distinction of autosomal dominant ichthyosis vulgaris and X-linked recessive ichthyosis

    • Ingrun Anton-Lamprecht
    • Mechtild Hofbauer

    Short Communications Pages: 261 - 264

11. Trisomy 14 in spontaneous abortus

    • Tadashi Kajii
    • Koso Ohama
    • Ariane Ferrier

    Short Communications Pages: 265 - 267

12. Dominant inheritance of absence of the breast

    • Miriam G. Wilson
    • E. B. Hall
    • Allan J. Ebbin

    Short Communications Pages: 268 - 270

13. The phosphoglucomutase (PGM₁)-groups in the Swiss population

    • R. Pflugshaupt
    • R. Scherz
    • R. Bütler

    Short Communications Pages: 271 - 273

14. Contribution to the genetics of serum β-lipoprotein in man

    • G. Morganti
    • P. E. Beolchini
    • A. Vierucci

    Short Communications Pages: 274 - 276

15. GPT, 6-PGD, PGM and AK phenotyping inone starch gel

    • H. Werner Goedde
    • Heide-G. Benkmann

    Short Communications Pages: 277 - 278

16. Adenosine deaminase (ADA) polymorphism in Northern England

    • S. S. Papiha
    • D. F. Roberts

    Short Communications Pages: 279 - 281

17. “Relatedness” between antibodies —Implications on immunogenetic systems

    • Jan Hirschfeld

    Short Communications Pages: 282 - 284

18. Giemsa banding in the D₁ trisomy syndrome

    • Charlotte Boone Halicioglu
    • Ergül Tuncbilek
    • Burhan Say

    Clinical Case Reports Pages: 285 - 286

19. A further case of basal cell nevus syndrome and structural chromosome abnormalities

    • Rudolf Happle
    • Angelika Kupferschmid

    Clinical Case Reports Pages: 287 - 288