Frequency of inborn errors of metabolism, especially PKU, in some representative newborn screening centers around the world O. Thalhammer Reviews Pages: 273 - 286
A subtelocentric chromosome 9 in a dysplastic 18-year-old boy with dissociated mental development I. HansmannJ. Keute Original Investigations Pages: 287 - 289
The Bf locus in the HLA region of chromosome 6: Linkage and association studies B. OlaisenP. TeisbergE. Thorsby Original Investigations Pages: 291 - 296
Obtention simultanée de plusieurs marquages chromosomiques sur les mêmes préparations, après traitement par le BrdU B. Dutrillaux Original Investigations Pages: 297 - 306
Trisomy 9p due to paternal translocation, t(9;13)(q13;q12) A. SchinzelK. HayashiW. Schmid Original Investigations Pages: 307 - 316
Sister chromatid exchanges and chromatid interchanges in Bloom's syndrome Traute M. Schroeder Original Investigations Pages: 317 - 323
A technique for in situ Karyotyping of primary amniotic fluid cell cultures W. Schmid Original Investigations Pages: 325 - 330
Climate associated variations in the human serum albumin level H. WalterB. Schöbel Original Investigations Pages: 331 - 335
DNA replication patterns of human C group chromosomes from fibroblasts and amniotic fluid cells revealed by a Giemsa staining technique J. T. EpplenW. Vogel Short Communications Pages: 337 - 339
Contribution to the genetics of serum β-lipoproteins in man G. MorgantiP. B. BeolchiniA. Vierucci Short Communications Pages: 341 - 342
Cytological and cytogenetical studies on brain tumors H. ZanklA. F. WeissK. D. Zang Short Communications Pages: 343 - 348
A comment to the paper: Dermatoglyphic analysis as a diagnostic tool in wilson disease? T. J. DavidA. B. Ajdukiewicz Letters to the Editor Pages: 349 - 349