A case of trisomy of the short arms of chromosome No. 4 with translocation t(4p 21p; 4q 21q) in the mother M. FurbettaG. RosiA. Cao Original Investigations Pages: 87 - 91
Twelve families with Hb 0 Arab in the Burgas district of Bulgaria observations on sixteen examples of Hb 0 β° thalassaemia K. N. KantchevB. N. TcholakovM. El Hazmi Original Investigations Pages: 93 - 97
Staining banded human chromosomes with Romanovsky dyes: Some practical consequences of the nature of the stain Diana J. CurtisRichard W. Horobin Original Investigations Pages: 99 - 104
Changes in the mitotic cycle induced by α-solanine David KirkUrsula Mittwoch Original Investigations Pages: 105 - 111
Prevalence of Edwards' syndrome. Clustering and seasonal variation? Johannes NielsenVagn HolmJørgen Haahr Short Communications Pages: 113 - 116
Complementation after fusion of Sandhoff- and Tay-Sachs fibroblasts H. H. RopersK. -H. GrzeschikErika Bühler Short Communications Pages: 117 - 121
Structural aberrations of chromosome 18 A. SchinzelK. HayashiW. Schmid Short Communications Pages: 123 - 132
Structural X-chromosome abnormality in a female with gonadal dysgenesis Herluf KristensenUrsula FriedrichAage Juhl Therkelsen Short Communications Pages: 133 - 138
Transspecific variability of red cell galactose 1-phosphate uridyl transferase in primates S. BissbortH. RitterJ. Schmitt Short Communications Pages: 139 - 141
Transspecific variability of soluble glutamic-pyruvic transaminase in Primates J. KömpfH. RitterJ. Schmitt Short Communications Pages: 143 - 146
Red cell glutamic-pyruvic transaminase gene frequencies in the region of the Po delta (Ferrara, Northern Italy) R. ScozzariG. TrippaP. Menini Short Communications Pages: 147 - 150
Zur Differenzierung der Varianten 5-1 und 6-1 im Adenosindesaminase-Polymorphismus. Nachweis des neuen Phänotyps ADA 5-2 in der ČSSR Georg RadamHansjürg StrauchBohdan Vavruša Kurze Originalmitteilungen Pages: 151 - 154
The effect of a thyrostatic drug on mitotic activity of human lymphocytes in vitro V. ZamrazilJ. NěmecL. Seidlová Short Communications Pages: 155 - 156
The phocomelia-thrombocytopenia syndrome. A follow-up report R. A. PfeifferC. Haneke Clinical Case Reports Pages: 157 - 158
XXYY son of a triple-X mother Jan ŽižkaPetr BalíčekJohannes Nielsen Clinical Case Reports Pages: 159 - 160
A girl with karyotype 46,XX,del(7) (qter→p15:) Ursula FriedrichTroels LyngbyeJakob Øster Clinical Case Reports Pages: 161 - 165
