Progress in visualization of eukaryotic gene transcription M. F. Trendelenburg Review Articles Pages: 197 - 215
Balanced structural changes involving the human X: Effect on sexual phenotype K. Madan Review Articles Pages: 216 - 221
A linkage study of acrokeratoelastoidosis. Possible mapping to chromosome 2 J. GreinerJ. KrügerF. Vogel Original Investigations Pages: 222 - 227
The Hellinger distance as used for the representation of serological ABO distances among earlier human populations F. Juhász Original Investigations Pages: 228 - 231
A cell surface abnormality in Duchenne muscular dystrophy: Intercellular adhesiveness of skin fibroblasts from patients and carriers G. E. JonesJ. A. Witkowski Original Investigations Pages: 232 - 237
NOR activity and satellite association patterns in a family carrying a doubly satellited marker Cathy M. TuckBrenda L. BordsonMaria Varela Original Investigations Pages: 238 - 240
Human red cell butyrylesterase, and its homologies in thirteen other mammalian species O. von DeimlingS. de Looze Original Investigations Pages: 241 - 246
Cell culture studies on neurofibromatosis (von Recklinghausen). II. Occurrence of glial cells in primary cultures of peripheral neurofibromas W. KroneG. JirikowskiH. Gall Original Investigations Pages: 247 - 251
Balanced translocations among couples with two or more spontaneous abortions: Are males and females equally likely to be carriers? A. Lippman-HandM. Vekemans Original Investigations Pages: 252 - 257
Evidence for the presence of β-subunit of hexosaminidase in a case of Sandhoff disease using a blotting technique Sophie GautronLivia PoenaruJean-Claude Dreyfus Original Investigations Pages: 258 - 261
Two-dimensional electrophoresis of soluble and structure-bound proteins from cultured human fibroblasts and hair root cells: Qualitative and quantitative variation J. KloseI. WillersH. W. Goedde Original Investigations Pages: 262 - 267
Meiotic behavior of alloxan-treated diabetic and nondiabetic T(1;13) 70H/+mice Paulette J. J. Wauben-PenrisJ. -B. Prins Original Investigations Pages: 268 - 273
Characterization of normal and abnormal variants of galactose-1-phosphate uridylyltransferase (EC 2.7.7.12) by isoelectric focusing R. I. KelleyH. HarrisW. J. Mellman Original Investigations Pages: 274 - 279
Polymorphism of erythrocyte galactose-1-phosphate uridyltransferase among Chinese Y. -K. XuW. G. Ng Original Investigations Pages: 280 - 282
Absence of correlation between Y chromosome heterochromatin and several anthropometric measurements in a Mexican population S. ArmendaresR. LiskerLizbeth Ruz Original Investigations Pages: 283 - 284
Cytogenetic effects of acetaldehyde in lymphocytes of Germans and Japanese: SCE, clastogenic activity, and cell cycle delay J. U. BöhlkeS. SinghH. W. Goedde Original Investigations Pages: 285 - 289
Demonstration of gene dosage effects for AK3 and GALT in fibroblasts from a fetus with 9p trisomy P. SteinbachR. Benz Short Communications Pages: 290 - 291
Genetic control of platelet glutaminase: A twin study Suman SahaiF. Vogel Short Communications Pages: 292 - 293
Segregation of a 22 ring chromosome in three generations C. StollM. -P. Roth Clinical Case Reports Pages: 294 - 296
A new inducible fragile site on chromosome 3(p14.2) in human lymphocytes R. -D. Wegner Clinical Case Reports Pages: 297 - 298
Coincidence between fragile site expression and interstitial deletion of chromosome 11 in a case of myelofibrosis M. SessaregoF. AjmarP. Boccaccio Clinical Case Reports Pages: 299 - 301
A simple method for R-banding combined with in situ hybridization A. BernheimR. Berger Letter Pages: 303 - 303