1. Gene activation during early development of mammals

   • U. Wolf
   • W. Engel

   Reviews 01 June 1972 Pages: 99 - 118

2. Inherited high serum levels of a functionally deficient complement esterase inhibitor associated with Hereditary Angioedema

   • F. Kueppers
   • U. Berendes
   • E. Schöpf

   Original Investigations 01 June 1972 Pages: 119 - 125

3. Syndrome de Lesch-Nyhan

   • A. M. Hagemeijer
   • P. Dodinval
   • J. M. Andrien

   Travaux Originaux 01 June 1972 Pages: 126 - 135

4. New data on the association between PTC and thyroid diseases

   • Heirie M. Mendez de Araújo
   • F. M. Salzano
   • Henry Wolff

   Original Investigations 01 June 1972 Pages: 136 - 144

5. Untersuchung über die Häufigkeiten angeborener Stoffwechselanomalien in Ost- und West-Österreich

   • O. Thalhammer
   • V. Scheiber

   Originalarbeiten 01 June 1972 Pages: 145 - 149

6. Cat-eye syndrome, a partial trisomy 22

   • Erica M. Bühler
   • Károly Méhes
   • Gerhard R. Stalder

   Original Investigations 01 June 1972 Pages: 150 - 162

7. Partielle Trisomie des kurzen Arms von Chromosom 4 mit Translokation 4p-,18q+ beim Vater

   • A. Schinzel
   • W. Schmid

   Originalarbeiten 01 June 1972 Pages: 163 - 171

8. Further studies on the distribution of some serum protein and enzyme groups in South India

   • R. Ananthakrishnan

   Original Investigations 01 June 1972 Pages: 172 - 176

9. Some notes on the geographical distribution of the human red cell acid phosphatase phenotypes

   • R. Ananthakrishnan
   • H. Walter

   Original Investigations 01 June 1972 Pages: 177 - 181

10. Polymorphismus der erythrocytären NADH-Diaphorase in der westdeutschen Bevölkerung

    • B. G. Potrafki
    • H. Hellenbroich
    • G. Pulverer

    Originalarbeiten 01 June 1972 Pages: 182 - 185

11. Red cell enzyme polymorphisms in Bulgaria

    • R. Ananthakrishnan
    • H. Walter
    • L. Tsacheva

    Original Investigations 01 June 1972 Pages: 186 - 190

12. A marker chromosome number 14 with double satellite observed in two generations: An unbalanced chromosome constitution associated with normal phenotype

    • F. Gigliani
    • A. de Capoa
    • A. Rocchi

    Original Investigations 01 June 1972 Pages: 191 - 195

13. Chromosome analysis of a primary carcinoma of the Fallopian tube

    • Wolfgang Weise
    • Heinz Herbert Büttner

    Clinical Case Reports 01 June 1972 Pages: 196 - 197

14. 1st der von F. Lenz beschriebene typus der Farbensinnstörung wirklich eine neue Varietät des Farbensinns?

    • W. Jaeger

    Briefe an die Herausgeber 01 June 1972 Pages: 198 - 200

15. Meine Antwort auf W. Jaegers brief an die herausgeber

    • F. Lenz

    Announcement 05 June 2004 Pages: 201 - 202