Defective decarboxylase in branched chain ketoacid oxidase multienzyme complex in classic type of maple syrup urine disease H. W. RüdigerU. LangenbeckL. Schuchmann Original Investigations Pages: 257 - 263
New families, onw with two recombinants for estimation of recombination between the Deutan and protan loci Sergio AriasAlvaro Rodríguez Original Investigations Pages: 264 - 268
Nucleoli and chromosomes: Their relationships during the meiotic prophase of the human fetal oocyte A. StahlJ. M. Luciani Original Investigations Pages: 269 - 284
Gonadendysgenesie mit ungewöhnlicher Strukturanomalie eines X-Chromosoms (45,X/46,XXq+) A. DollmannW. NockeSabine Stengel-Rutkowski Originalarbeiten Pages: 285 - 299
C 11/D 13-translocation in four generations H.-D. RottG. SchwanitzG. Alexandrow Original Investigations Pages: 300 - 305
The lymphocyte as a dosimeter: Comparison of somatic chromosome aberrations in 522 newborn infants and 602 mothers Shivanand R. PatilFrank H. RuddleHerbert A. Lubs Original Investigations Pages: 306 - 313
Hp, Gc, Cp, Tf, Bg and Pi phenotypes in leprosy patients and healthy controls from West Bengal (India) H. WalterG. KellermannM. R. Chakravartti Original Investigations Pages: 314 - 325
Contribution to the AK and 6-PGD polymorphism in prague P. HerzogJ. BohatováA. Drdová Short Communications Pages: 326 - 326
Constitutive heterochromatin patterns of G-group chromosomes in Down's syndrome Sen PathakAnil K. Sinha Short Communications Pages: 327 - 329
Polymorphism of erythrocyte phosphoglucomutase, adenylate kinase and adenosine deaminase in northern Thailand N. SanpitakH. DelbrückG. Flatz Short Communications Pages: 330 - 332
A modified method of culturing human amniotic fluid cells for prenatal detection of genetic disorders Henriette Knörr-GärtnerInge Härle Short Communications Pages: 333 - 334
