Inversion of ‘fluorescent’ segment in chromosome 3: A polymorphic trait D. SoudekHelena Sroka Original Investigations Pages: 109 - 115
Genetic studies on the Gc subtypes H. CleveW. PatutschnickG. G. Wendt Original Investigations Pages: 117 - 122
On the peripheral location of the Y chromosome Charles J. KowalskiC. E. NasjletiBecky Schmitt Original Investigations Pages: 123 - 135
Sister chromatid exchange in lymphocytes from patients with malignant lymphoma Karen KurvinkClara D. BloomfieldJaroslav Cervenka Original Investigations Pages: 137 - 144
Familial and sporadic porphyria cutanea H. de VerneuilG. AitkenY. Nordmann Original Investigations Pages: 145 - 151
Sister chromatid exchanges in the peripheral blood of cigarette smokers and in lung cancer patients; and the effect of chemotherapy D. H. HollanderM. S. TockmanJ. K. Frost Original Investigations Pages: 165 - 171
Rapid identification of chromosomes carrying silver-stained nucleolus-organizing regions C. H. C. M. BuysJ. OsingaG. J. P. A. Anders Original Investigations Pages: 173 - 180
Isozyme variations in acetaldehyde dehydrogenase (E.C.1.2.1.3) in human tissues Shoji HaradaDharam P. AgarwalH. W. Goedde Original Investigations Pages: 181 - 185
Suppression of the frequencies of sister chromatid exchanges in Bloom's syndrome fibroblasts by co-cultivation with Chinese hamster cells P. P. W. van BuulA. T. NatarajanElly A. M. Verdegaal-Immerzeel Short Communications Pages: 187 - 189
Origin of mitotic cells of the chorionic villi in direct chromosome analysis Masatomo WatanabeTakashi ItoGen-ichi Watanabe Short Communications Pages: 191 - 193
Partial monosomy of the short arm of chromosome 9 J. DerooverJ. P. FrynsH. van den Berghe Clinical Case Reports Pages: 195 - 200
Partial trisomy 18q in a newborn with typical 18 trisomy phenotype J. P. FrynsF. DetavernierH. van den Berghe Clinical Case Reports Pages: 201 - 205
Mosaicism for an additional partial chromosome 8: 46,XX/47,XX+der(8)(p21→qter) R. A. PfeifferE. KesselT. Nehring Clinical Case Reports Pages: 207 - 212
Un cas de rétinoblastome bilatéral avec monosomie 13 partielle (q12→q14) Roland WalbaumPierre FrançoisGilberte Delassus Clinical Case Reports Pages: 219 - 226