Translocation (13q21q) Margareta MikkelsenA. HanssonN. Hobolth Original Investigations Pages: 303 - 307
Über einen Fall von atypischer Galaktosämie Dieter MatzJörg EnzenauerFritz Menne Original Investigations Pages: 309 - 313
Heterozygote tests and genetic counseling in Maple Syrup Urine Disease U. LangenbeckT. GrimmE. Passarge Original Investigations Pages: 315 - 322
Rapid determination of hypoxanthine-guanine-phosphoribosyl transferase in human fibroblasts and amniotic cells I. WillersD. P. AgarwalH. W. Goedde Original Investigations Pages: 323 - 328
X monosomy and 21 trisomy in a sibship Antoine BroustetFrançoise ServilleMonique Gachet Short Communications Pages: 333 - 337
Non-random appearance of Y-chromatin-like fluorescence in the nuclei of thyroid and brain and its chromosomal background M. SellyeiL. VassT. Krausz Short Communications Pages: 339 - 342
Esterase-D polymorphism in Assam by cellulose acetate electrophoresis Heide -G. BenkmannH. Werner Goedde Short Communications Pages: 343 - 345
Haemoglobin Norfolk in Nepali Gorkhas T. N. MehrotraS. C. GuptaB. G. Wiltshire Short Communications Pages: 347 - 349
Trisomy 21 and trisomy 18 in half-siblings T. J. DavidA. J. Jones Clinical Case Reports Pages: 351 - 352
A case of trisomy 9p in a family with translocation 9/15 Petr BalíĉekJan ŽižkaJosef Lichý Clinical Case Reports Pages: 353 - 358