Assignment of NADH-cytochrome b5 reductase (DIA1 locus) to human chromosome 22 Claudine JunienMagdeleine VibertJean-Claude Kaplan Original Investigations Pages: 233 - 239
The transition in frequency of Y chromatin in males during the neonatal period Kumiko IijimaMakoto HigurashiMunehiro Hirayama Original Investigations Pages: 241 - 243
Silver stain reveals nucleolus organizer regions on a satellited Yq chromosome W. Mike HowellPatricia N. Howard-PeeblesGayle R. Stoddard Original Investigations Pages: 245 - 250
Trisomy 9p and unusual translocation mongolism in siblings due to different 3:1 segregations of maternal translocation rcp(9;21)(p11;q11) Manfred HabedankJoachim Faust Original Investigations Pages: 251 - 256
Variability and familial transmission of constitutive heterochromatin of human chromosomes evaluated by the method of linear measurement Petr BalíčekJan ŽižkaHana Skalská Original Investigations Pages: 257 - 265
10q(q23→qter) duplication: GOTs, HK1, and other gene markers Robert S. SparkesHarold N. BassMaryellen C. Sparkes Original Investigations Pages: 267 - 270
Study of human male meiosis II-Q-banding in pachytene bivalents M. L. de TorresJ. A. Abrisqueta Original Investigations Pages: 283 - 289
Comparison of silver staining of nucleolus organizer regions in human lymphocytes and fibroblasts A. -V. MikelsaarH. G. Schwarzacher Original Investigations Pages: 291 - 299
Genetic polymorphism of the second component of human complement (C2) B. OlaisenP. TeisbergE. Thorsby Original Investigations Pages: 301 - 305
Furrows and dermal ridges of the hand in patients with alcohol embryopathy I. TillnerF. Majewski Original Investigations Pages: 307 - 314
Evidence for a ‘silent allele’ GLO 0 at the glyoxalase I locus Ch. RittnerW. Weber Short Communications Pages: 315 - 318
Time and cell systems as variables in fusion experiments with polyethylene glycol G. J. P. A. AndersJoke WierdaVera J. S. Idenburg Short Communications Pages: 319 - 322
Trisomy-8 mosaicism: Report of a case Margherita Cirillo SilengoGianfranco DaviPiergiorgio Franceschini Clinical Case Reports Pages: 323 - 326
Patau's syndrome and 13q21q translocation Amalia Pérez-CastilloJ. A. Abrisqueta Clinical Case Reports Pages: 327 - 331
Terminal deletion of the long arm of chromosome 1 in a malformed newborn E. KesselR. A. PfeifferJ. Schwarz Clinical Case Reports Pages: 333 - 337
Partial deletion 10q Raymond C. Lewandowski Jr.Mary K. KukolichCarl B. Mankinen Clinical Case Reports Pages: 339 - 343
Ring chromosome 3 in a retarded boy Regine WitkowskiEva UllrichUrsula Piede Clinical Case Reports Pages: 345 - 348
Balanced reciprocal whole-arm translocation t(1;19) in three generations Anne M. SchoberChrista Fonatsch Clinical Case Reports Pages: 349 - 352