Altered cellular response to UV irradiation in a patient affected by premature ageing Miria StefaniniG. OrecchiaFiorella Nuzzo Original Investigations Pages: 189 - 192
The human ribosomal RNA genes: structure and organization of the complete repeating unit J. E. SylvesterD. A. WhitemanR. D. Schmickel Original Investigations Pages: 193 - 198
Increased spindle resistance to antimicrotubule agents in women of high risk for meiotic nondisjunction Aviva DotanLydia Avivi Original Investigations Pages: 199 - 204
Paracentric inversions in man J. P. FrynsA. KleczkowskaH. Van den Berghe Original Investigations Pages: 205 - 213
Free N-acetylneuraminic acid (NANA) storage disorders: evidence for defective NANA transport across the lysosomal membrane G. M. S. ManciniF. W. VerheijenH. Galjaard Original Investigations Pages: 214 - 217
Ring chromosome 21 in healthy persons: different consequencies in females and in males B. DallapiccolaV. De FilippisL. Zelante Original Investigations Pages: 218 - 220
Different ζ globin gene deletions among Black Americans A. E. FeliceM. P. CleekT. H. J. Huisman Original Investigations Pages: 221 - 224
Direct regional assignment of the gene for vitamin D binding protein (Gc-globulin) to human chromosome 4q11-q13 and identification of an associated DNA polymorphism Nancy E. CookeH. F. WillardDonna L. George Original Investigations Pages: 225 - 229
Tentative assignment of piebald trait gene to chromosome band 4q12 J. J. HooR. H. A. HaslamC. van Orman Original Investigations Pages: 230 - 231
Familial fragile site found at the cancer breakpoint (1)(q32) Fiorella ShabtaiJ. HartI. Halbrecht Original Investigations Pages: 232 - 234
Juvenile Huntington disease J. G. van DijkE. A. van der VeldeG. W. Bruyn Original Investigations Pages: 235 - 239
Haplotypes of the human apoprotein AI-CIII-AIV gene cluster in coronary atherosclerosis G. A. A. FernsD. J. Galton Original Investigations Pages: 245 - 249
Two-dimensional gel analysis of proteins from human trisomy 21 fetal liver tissue after DEAE-Sepharose chromatography G. H. Reichert Original Investigations Pages: 250 - 253
The chromosome breakpoint at 14q32 in an ataxia telangiectasia t(14;14) T cell clone is different from the 14q32 breakpoint in Burkitts and an inv(14) T cell lymphoma A. A. KennaughS. V. ButterworthA. M. R. Taylor Original Investigations Pages: 254 - 259
Telomeric fusion in pre-T-cell acute lymphoblastic leukemia R. MorganV. JarzabekA. A. Sandberg Original Investigations Pages: 260 - 263
Linkage studies of X-linked recessive spastic paraplegia using DNA probes S. KenwrickV. IonasescuK. E. Davies Original Investigations Pages: 264 - 266
Mapping of human X-linked hypophosphataemic rickets by multilocus linkage analysis A. P. ReadR. V. ThakkerJ. L. H. O'Riordan Original Investigations Pages: 267 - 270
X-linked dominant hypophosphatemia is closely linked to DNA markers DXS41 and DXS43 at Xp22 M. MächlerD. FreyW. Schmid Original Investigations Pages: 271 - 275
Esterase D polymorphism in a French-Canadian population L. CoutureMonique ChagnonC. Bouchard Short Communications Pages: 276 - 276
Assignment of human uroporphyrinogen decarboxylase (URO-D) to the p34 band of chromosome 1 A. DubartM. G. MatteiM. Goossens Short Communications Pages: 277 - 279