Genetics and biochemistry of the phenylketonuria-present state K. Bartholomé Review Articles Pages: 241 - 245
Demonstration of two different regions of lateral asymmetry in human Y chromosomes J. LimonZ. GibasTeresa Moruzgala Original Investigations Pages: 247 - 252
Cytogenetic effects of inactivated influenza virus on male germ cells of mice Meneka A. ThadaniHanumanlu Polasa Original Investigations Pages: 253 - 258
Assignment of structural β-galactosidase loci to human chromosomes 3 and 22 J. de WitH. L. HoeksemaA. Westerveld Original Investigations Pages: 259 - 267
C-band polymorphisms of chromosomes 1, 9, and 16 in four subgroups of mentally retarded patients and a normal control population H. S. WangJ. L. Hamerton Original Investigations Pages: 269 - 275
Partial translocation of NOR and its activity in a balanced carrier and in her cri-du-chat fetus V. G. DevJanice ByrneGloria Bunch Original Investigations Pages: 277 - 280
Populational polymorphisms in silver staining of nucleolus organizer regions (NORs) in human acrocentric chromosomes A. -V. MikelsaarT. Ilus Original Investigations Pages: 281 - 285
Polymorphism of alanine aminotransferase (E.C.2.7.6.1): Common and rare alleles J. KömpfH. Ritter Original Investigations Pages: 287 - 292
Genetic polymorphism of α-L-fucosidase in brittany (France) I. Trinh-Dinh-KhoiD. GlaiseJ. Y. Le Gall Original Investigations Pages: 293 - 296
Incidence and characteristics of glucose-6-phosphate dehydrogenase variants in Japan Tadako NakatsujiShiro Miwa Original Investigations Pages: 297 - 305
Haplotype analysis of the linkage group HLA-A: HLA-B: Bf in Japanese Satoshi HoraiTakeo JujiHachiro Nakajima Original Investigations Pages: 307 - 314
Deficiency of arginine and lysine causes increase in the frequency of sister chromatid exchanges W. SchemppW. Krone Short Communications Pages: 315 - 318
Mitochondrial malic enzyme (E.C. 1.1.1.40) in human leukocytes: Formal genetics and population genetics G. SiebertH. RitterJ. Kömpf Short Communications Pages: 319 - 322
Common polymorphism of peptidase A: Formal genetics and population data J. KömpfG. SiebertH. Ritter Short Communications Pages: 323 - 325
Human mitochondrial glutamic-oxaloacetic-transaminase, GOTM: Formal genetics H. RitterJ. Kömpf Short Communications Pages: 327 - 329
Racial differences in alcohol sensitivity: A new hypothesis H. W. GoeddeS. HaradaD. P. Agarwal Short Communications Pages: 331 - 334
A new case of partial trisomy 15q- A. GeneixJ. Y. JaffrayP. Crost Clinical Case Reports Pages: 335 - 338
A low frequency mosaicism for monosomy 21 in a live born female Ming-liang LeeDemetra RoseL. J. Sciorra Clinical Case Reports Pages: 343 - 347
Partial trisomy of 11 and 22 due to familial translocation t(11;22) (q23;q11), inherited in three generations Hiroshi NakaiYoshifumi YamamotoYoshikazu Kuroki Clinical Case Reports Pages: 349 - 355