Polymorphism of α1-antitrypsin in a Portuguese population Helena Manuela GeadaJ. A. Pereira AlbinoCarlos Manso Original Investigations Pages: 109 - 113
Frequency of chromosomal fluorescence polymorphism in normal persons and in clinical patients with diagnosed chromosome aberrations Eberhard SchwingerHeinz Wehner Original Investigations Pages: 115 - 119
Ss blood Group Associated PAS-staining polymorphism of glycoprotein 3 from human erythrocyte membranes W. DahrG. UhlenbruckE. Janßen Original Investigations Pages: 121 - 132
Partial and complete trisomy 9: Delineation of a trisomy 9 syndrome Grant R. SutherlandRodney F. CarterLloyd L. Morris Original Investigations Pages: 133 - 140
Distribution of spontaneous chromosome breaks in human chromosomes Pertti AulaHarriet von Koskull Original Investigations Pages: 143 - 148
Morphologic variability of human chromosomes: Polymorphism of constitutive heterochromatin P. K. GhoshIndera P. Singh Original Investigations Pages: 149 - 154
Banding of human chromosomes with basic fuchsin J. M. J. C. ScheresG. F. M. Merkx Original Investigations Pages: 155 - 169
GD (-) Aachen, a new variant of deficient glucose-6-phosphate dehydrogenase Axel KahnAlbrecht EstersManfred Habedank Original Investigations Pages: 171 - 180
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. PropertColin J. Brackenridge Original Investigations Pages: 181 - 188
Evidenz für eine Mosaikstruktur der Netzhaut bei Konduktorinnen für Dichromasie Gerhard BornPeter GrütznerHansjörg Hemminger Original Investigations Pages: 189 - 196
Confirmation of linkage between the loci for HL-A and glyoxalase I J. KömpfS. BissbortF. Schunter Short Communications Pages: 197 - 198
Increased sister chromatid exchange events in the human late replicating X W. SchnedlW. PumbergerH. G. Schwarzacher Short Communications Pages: 199 - 202
Cell selection in vivo in normal/aneuploid chromosome abnormalities Johannes Nielsen Short Communications Pages: 203 - 206
Tricho-rhino-phalangeal syndrome Naoki FukushimaMichiya AnakuraTadashi Ohsawa Clinical Case Reports Pages: 207 - 210
Pathomorphological changes in an early spontaneous abortus with triploidy (69,XXX) V. P. KulazenkoL. G. Kulazenko Clinical Case Reports Pages: 211 - 215
Trisomy 9p resulting from maternal 9/21 translocation I. ŠubrtBohunka BlehováBlanka Pallová Clinical Case Reports Pages: 217 - 220
Exomphalos and trisomy 18 syndrome Jan ŽižkaPetr BalíčekMarie Koďousková Clinical Case Reports Pages: 221 - 223
Etude chromosomique et clinique d'une fillette porteuse d'une deletion (2) (q34q36) Stéphanie WarterCharles LauseckerAdrien Pennerath Clinical Case Reports Pages: 225 - 227
A new translocation in chronic myelogenous leukemia D. PravtchevaP. AndreevaR. Tsaneva Clinical Case Reports Pages: 229 - 232
