1. Cat Eye-Syndrom

   • J. Kunze
   • M. Tolksdorf
   • H.-R. Wiedemann

   Übersichtsartikel Pages: 271 - 289

2. Parakeratosis Mibelli and skin carcinoma

   • E. A. Goerttler
   • E. G. Jung

   Review Pages: 291 - 296

3. Chromosome studies in patients with congenital malformations and mental retardation

   • B. Erdtmann
   • F. M. Salzano
   • Margarete S. Mattevi

   Original Investigations Pages: 297 - 306

4. Chromosomale Instabilität bei Homo- und Heterozygotie für mikrocephalia vera

   • W. Vormittag
   • E. Kunze-Mühl
   • M. Weninger

   Originalarbeiten Pages: 307 - 314

5. Constitutive heterochromatin and micronucleoli in the human oocyte at the diplotene stage

   • A. Stahl
   • J. M. Luciani
   • R. Gagné

   Original Investigations Pages: 315 - 327

6. Satellite DNA III and alkaline Giemsa staining

   • Erica M. Bühler
   • Taiso Tsuchimoto
   • Gerhard R. Stalder

   Original Investigations Pages: 329 - 333

7. G banding in cytogenetic study of hemoblastoses

   • E. W. Fleischman
   • E. L. Prigogina

   Original Investigations Pages: 335 - 342

8. Del(10)p autosomal deletion syndrome: Clinical, cytogenetic and gene marker studies

   • Uta Francke
   • Carol Kernahan
   • Christy Bradshaw

   Short Communications Pages: 343 - 351

9. High amniotic fluid alpha-1-fetoprotein in a case of fetal sacrococcygeal teratoma

   • W. Schmid
   • J. P. Mühlethaler

   Clinical Case Reports Pages: 353 - 354

10. Meiotic chromosome study in a human female translocation heterozygote

    • B. Uebele-Kallhardt
    • K. Knörr

    Clinical Case Reports Pages: 355 - 356