Potential genetic functions of tandem repeated DNA sequence blocks in the human genome are based on a highly conserved “chromatin folding code” Peter Vogt Review Article Pages: 301 - 336
A new glucose-6-phosphate dehydrogenase variant with congenital nonspherocytic hemolytic anemia (G6PD Genova) Gian Franco GaetaniSilvana GalianoAnna Maria Ferraris Original Investigations Pages: 337 - 340
Assignment by in situ hybridization of the angiotensinogen gene to chromosome band 1q4, the same region as the human renin gene I. Gaillard-SanchezM. G. MatteiP. Corvol Original Investigations Pages: 341 - 343
Frequency and effect of human apolipoprotein A-IV polymorphism on lipid and lipoprotein levels in an Icelandic population Hans-Jürgen MenzelGunnar SigurdssonGerd Utermann Original Investigations Pages: 344 - 346
Unusual X chromosome inactivation in a mentally retarded girl with an interstitial deletion Xq27: implications for the fragile X syndrome Malgorzata SchmidtAndrea CertomaDavid M. Danks Original Investigations Pages: 347 - 352
Lymphocyte and sperm chromosome studies in cancer-treated men A. GenescàL. BarriosJ. Egozcue Original Investigations Pages: 353 - 355
A possible common origin of “Y-negative” human XX males and XX true hermaphrodites Nacer Eddine AbbasJean Edmond ToublancMarc Fellous Original Investigations Pages: 356 - 360
Mitotic disturbance associated with mosaic aneuploidies K. MillerW. MüllerSibylle D. Flatz Original Investigations Pages: 361 - 364
Hb D Los Angeles (D-Punjab) and Hb Presbyterian: analysis of the defect at the DNA level J. SchneeC. Aulehla-ScholzJ. Horst Original Investigations Pages: 365 - 367
Genetic studies on human thyroxine-binding globulin (TBG) C. LuckenbachJ. KömpfH. Ritter Short Communications Pages: 368 - 370
Replication studies in the 16p+ variant P. W. ThompsonS. H. RobertsS. M. Rees Short Communications Pages: 371 - 372
An insertion deletion polymorphism in the signal peptide of the human apolipoprotein B gene Sophia VisvikisLawrence ChanEric Boerwinkle Short Communications Pages: 373 - 375
Attempt to calculate the allele frequency distribution of a TaqI RFLP detected by the highly polymorphic probe YNH24 P. H. van EedeT. M. CuypersG. G. de Lange Short Communications Pages: 376 - 378
Linkage disequilibrium between cystic fibrosis locus and three DNA markers, XV-2c, KM19 and MP6d-9, in 43 Spanish families Esther FernándezJavier BenitezCarmen Ramos Letters to the Editors Pages: 379 - 380
Definition of an acquired 11q deletion in a tumorigenic human monocytic cell line Emanuela MaseratiLorenza RomittiR. Revoltella Letters to the Editors Pages: 381 - 381
