1. The G-banded prophase chromosomes of man

   • Jorge J. Yunis
   • Otto Sanchez

   Original Investigations Pages: 167 - 172

2. Linkage group HL-A-MLC-Bf (properdin factor B)

   • Ch. Rittner
   • H. Grosse-Wilde
   • E. D. Albert

   Original Investigations Pages: 173 - 183

3. Lipoproteins in lecithin-cholesterol-acyltransferase (LCAT)^*-deficiency

   • G. Utermann
   • H. J. Menzel
   • P. Dieker

   Original Investigations Pages: 185 - 197

4. Centronucleäre Myopathie mit autosomal dominantem Erbgang

   • W. Mortier
   • E. Michaelis
   • L. Gerhard

   Original Investigations Pages: 199 - 215

5. Enzyme polymorphisms and haemoglobin variants in Greeks

   • P. Schneider
   • R. Ananthakrishnan
   • R. Abele

   Original Investigations Pages: 217 - 222

6. Three cases of minor chromosomal aberrations discovered by prenatal chromosome determination

   • Jan Wahlström

   Short Communications Pages: 223 - 225

7. Frequency and distribution of sister-chromatid exchanges in a case of Fanconi's anemia

   • K. Sperling
   • R.-D. Wegner
   • G. Obe

   Short Communications Pages: 227 - 230

8. Hereditary defect of the sacrum

   • Burhan Say
   • James G. Coldwell

   Short Communications Pages: 231 - 234

9. Red blood cell acid phosphatase: Ambiguity in phenotype and activity estimations in the proof of the “single allele” states

   • Otomar Pihar

   Short Communications Pages: 235 - 240

10. Etude méiotique et mitotique dans un cas de translocation t(5;Y)

    • B. Dutrillaux
    • J. Gueguen

    Short Communications Pages: 241 - 245

11. G-6PD “ankara”. A new G-6PD variant with deficiency found in a Turkish family

    • Axel Kahn
    • M. L. North
    • P. Boivin

    Short Communications Pages: 247 - 250

12. Dicentric Yp chromosome in a patient with the gonadal dysgenesis and gonadoblastoma

    • J. Málková
    • K. Michalová
    • L. Stárka

    Clinical Case Reports Pages: 251 - 253

13. Deletion of long arms of chromosome 13

    • M. Kučerová
    • Z. Polívková
    • M. Pokorná

    Clinical Case Reports Pages: 255 - 257

14. Ring chromosome 15:r(15). Identification by R banding

    • C. Stoll
    • J. G. Juif
    • C. Lausecker

    Clinical Case Reports Pages: 259 - 262

15. Balanced familial translocation t(5;19) (q12;p or q11) with phenotypical abnormalities in a girl

    • Claude Stoll
    • Jean-Marc Levy
    • Maxime Champy

    Clinical Case Reports Pages: 263 - 267

16. Trisomy 9p in a girl whose mother has a translocation t(9;20)(q12;p13)

    • Claude Stoll
    • Jean-Marc Levy
    • Alexandre Gardea

    Clinical Case Reports Pages: 269 - 274