Antenatal sex determination in blood from pregnant women J. W. SiebersIlse KnaufW. Vogel Original Investigations Pages: 273 - 280
Dermatoglyphic analysis as a diagnostic tool in Wilson disease? R. Grosse Original Investigations Pages: 281 - 284
Some hereditary blood factors of the Bengali Muslim of Bangladesh (red cell enzymes, haemoglobins, and serum proteins) S. S. PapihaD. F. RobertsM. M. Islam Original Investigations Pages: 285 - 293
The human leukocyte test system Günter ObeBernd BeekGertrud Dudin Original Investigations Pages: 295 - 302
Relative position of trypsin banded homologous chromosomes in human (♀) metaphase figures Luc HensM. Kirsch-VoldersH. Galperin-Lemaître Short Communications Pages: 303 - 311
Three chromosome abnormalities (trisomy 21,XXY, and a de novo reciprocal translocation) in a child with 48,XXY,+21,t(6;10)(p22-24;p12) Philip D. Buchanan Short Communications Pages: 313 - 316
International registry of Abnormal Karyotypes D. S. BorgaonkarD. R. Bolling Short Communications Pages: 317 - 318
Phenylketonuria in a patient with cystinuria R. MinamiK. OlekP. Wardenbach Short Communications Pages: 319 - 324
Haemoglobin G Szuhu β80 asn → lys in an English family S. G. Welch Short Communications Pages: 331 - 333
Trisomie partielle 11q et translocation familiale 11–22 F. GiraudJ. -F. MatteiR. Bernard Clinical Case Report Pages: 343 - 347
Recurrent abortions and paternal balanced translocation t(1q-;13q+) Danuta RożynkowaBarbara Tr⪟bicka-KwiatkowskaAndrzej Krzemiński Clinical Case Report Pages: 349 - 351
The Tetraphocomelia-cleft palate syndrome F. R. GrosseC. PandelH. R. Wiedemann Clinical Case Report Pages: 353 - 356
Balanced homologous translocation t(22q22q) in a phenotypically normal woman with repeated spontaneous abortions L. M. S. FarahH. R. de S. NazarethD. Delascio Clinical Case Report Pages: 357 - 360
A comment to the paper: A homozygote for a serum albumin variant of the slow type J. -P. MartinC. Ropartz Letters to the Editor Pages: 361 - 361