1. Polymorphism of α₁-antitrypsin in a Portuguese population

   • Helena Manuela Geada
   • J. A. Pereira Albino
   • Carlos Manso

   Original Investigations Pages: 109 - 113

2. Frequency of chromosomal fluorescence polymorphism in normal persons and in clinical patients with diagnosed chromosome aberrations

   • Eberhard Schwinger
   • Heinz Wehner

   Original Investigations Pages: 115 - 119

3. Ss blood Group Associated PAS-staining polymorphism of glycoprotein 3 from human erythrocyte membranes

   • W. Dahr
   • G. Uhlenbruck
   • E. Janßen

   Original Investigations Pages: 121 - 132

4. Partial and complete trisomy 9: Delineation of a trisomy 9 syndrome

   • Grant R. Sutherland
   • Rodney F. Carter
   • Lloyd L. Morris

   Original Investigations Pages: 133 - 140

5. Chromosome measurements on an XXp+ male

   • Kamlesh Madan

   Original Investigations Pages: 141 - 142

6. Distribution of spontaneous chromosome breaks in human chromosomes

   • Pertti Aula
   • Harriet von Koskull

   Original Investigations Pages: 143 - 148

7. Morphologic variability of human chromosomes: Polymorphism of constitutive heterochromatin

   • P. K. Ghosh
   • Indera P. Singh

   Original Investigations Pages: 149 - 154

8. Banding of human chromosomes with basic fuchsin

   • J. M. J. C. Scheres
   • G. F. M. Merkx

   Original Investigations Pages: 155 - 169

9. GD (-) Aachen, a new variant of deficient glucose-6-phosphate dehydrogenase

   • Axel Kahn
   • Albrecht Esters
   • Manfred Habedank

   Original Investigations Pages: 171 - 180

10. The relation of sex, age, smoking status, birth rank and parental ages to pseudocholinesterase activity and phenotypes in a sample of Australian Caucasian adults

    • David N. Propert
    • Colin J. Brackenridge

    Original Investigations Pages: 181 - 188

11. Evidenz für eine Mosaikstruktur der Netzhaut bei Konduktorinnen für Dichromasie

    • Gerhard Born
    • Peter Grützner
    • Hansjörg Hemminger

    Original Investigations Pages: 189 - 196

12. Confirmation of linkage between the loci for HL-A and glyoxalase I

    • J. Kömpf
    • S. Bissbort
    • F. Schunter

    Short Communications Pages: 197 - 198

13. Increased sister chromatid exchange events in the human late replicating X

    • W. Schnedl
    • W. Pumberger
    • H. G. Schwarzacher

    Short Communications Pages: 199 - 202

14. Cell selection in vivo in normal/aneuploid chromosome abnormalities

    • Johannes Nielsen

    Short Communications Pages: 203 - 206

15. Tricho-rhino-phalangeal syndrome

    • Naoki Fukushima
    • Michiya Anakura
    • Tadashi Ohsawa

    Clinical Case Reports Pages: 207 - 210

16. Pathomorphological changes in an early spontaneous abortus with triploidy (69,XXX)

    • V. P. Kulazenko
    • L. G. Kulazenko

    Clinical Case Reports Pages: 211 - 215

17. Trisomy 9p resulting from maternal 9/21 translocation

    • I. Šubrt
    • Bohunka Blehová
    • Blanka Pallová

    Clinical Case Reports Pages: 217 - 220

18. Exomphalos and trisomy 18 syndrome

    • Jan Žižka
    • Petr Balíček
    • Marie Koďousková

    Clinical Case Reports Pages: 221 - 223

19. Etude chromosomique et clinique d'une fillette porteuse d'une deletion (2) (q34q36)

    • Stéphanie Warter
    • Charles Lausecker
    • Adrien Pennerath

    Clinical Case Reports Pages: 225 - 227

20. A new translocation in chronic myelogenous leukemia

    • D. Pravtcheva
    • P. Andreeva
    • R. Tsaneva

    Clinical Case Reports Pages: 229 - 232