1. The quantitative analysis of polymorphism on human chromosomes 1, 9, 16, and Y

   • O. A. Podugolnikova
   • I. V. Parfenova
   • A. A. Prokofieva-Belgovskaja

   Original Investigations Pages: 243 - 250

2. The quantitative analysis of polymorphism on human chromosomes 1, 9, 16, and Y

   • O. A. Podugolnikova
   • H. M. Sushanlo
   • A. A. Prokofieva-Belgovskaja

   Original Investigations Pages: 251 - 260

3. The quantitative analysis of polymorphism on human chromosomes 1, 9, 16, and Y

   • O. A. Podugolnikova

   Original Investigations Pages: 261 - 268

4. Short rib-polydactyly syndrome, Majewski type, in two male siblings

   • T. Motegi
   • M. Kusunoki
   • N. Mohri

   Original Investigations Pages: 269 - 275

5. Patial trisomy 1 due to 1/17 translocation in Ph'-Positive chronic myelocytic leukemia

   • F. Pasquali
   • D. Francesconi
   • G. Ippoliti

   Original Investigations Pages: 277 - 282

6. Partial trisomy for the long arm of chromosome 7 due to familial balanced translocation

   • M. Schmid
   • J. Wolf
   • W. Krone

   Original Investigations Pages: 283 - 289

7. G-banding patterns of high-resolution human chromosomes 6–22, X, and Y

   • J. J. Yunis
   • D. W. Ball
   • J. R. Sawyer

   Original Investigations Pages: 291 - 306

8. Simultaneous staining of sister chromatid exchanges and Q-bands in human chromosomes after treatment with methyl methane sulphonate, quinacrine mustard, and quinacrine

   • Ulla Haglund
   • Lore Zech

   Original Investigations Pages: 307 - 317

9. Evidence for a correlation between late replication and autosomal gene inactivation in a familial translocation t(X;21)

   • J. Couturier
   • B. Dutrillaux
   • E. Maillard

   Original Investigations Pages: 319 - 326

10. Chromosome lesions in amniotic fluid cell cultures

    • G. Simoni
    • L. Larizza
    • L. De Carli

    Original Investigations Pages: 327 - 332

11. Intracellular phenylalanine and tyrosine concentrations in 19 heterozygotes for phenylketonuria (PKU) and 26 normals

    • O. Thalhammer
    • G. Lubec
    • Helga Königshofer

    Original Investigations Pages: 333 - 336

12. Associations between atopic diseases and the polymorphic systems ABO, kidd, inv and red cell acid phosphatase

    • R. Brachtel
    • H. Walter
    • Maria Hilling

    Original Investigations Pages: 337 - 348

13. Biochemical genetic markers in the Kadazans of Sabah, Malaysia

    • S. G. Tan
    • Y. -S. Teng
    • L. E. Lie-Injo

    Original Investigations Pages: 349 - 353

14. Genetic variation in parotid basic proteins (Pb) in the Bozo (Mali, West Africa)

    • G. Pals
    • J. C. Pronk

    Short Communications Pages: 355 - 359

15. Partial trisomy 17q

    • J. P. Fryns
    • C. Parloir
    • H. Van den Berghe

    Clinical Case Reports Pages: 361 - 364