The behavior of ring chromosome 13 J. J. HooU. ObermannH. Cramer Original Investigations Pages: 161 - 171
Les IgG dans les aberrations chromosomiques: Étude familiale de l'expression quantitative des allotypes du système Gm et de certaines sous-classes d'IgG Liliane RivatMaryvonne DaveauC. Ropartz Travaux Originaux Pages: 173 - 190
Monosomy for the centromeric and juxtacentromeric region of chromosome 21 Søren HolbekUrsula FriedrichGert Bruun Petersen Short Communications Pages: 191 - 195
Tentative localization of a Hageman (factor XII) locus on 7q, probably the 7q35 band J. de GrouchyC. TurleauJacqueline Nedelec Short Communications Pages: 197 - 200
Dermatoglyphics in trisomy 8 mosaicism Blanka SchaumannJaroslav CervenkaRobert J. Gorlin Short Communications Pages: 201 - 205
The evolution of the Phl-trisomic clone, in a case of chronic myeloid leukemia M. Hussein Khan Short Communications Pages: 207 - 212
The human red cell acid phosphatase activity and its statistical evaluation K. BergR. KamelH. Wischerath Short Communications Pages: 213 - 215
1q+ variants in a normal adult population (one with a pericentric inversion) S. TüürM. KäosaarA. -V. Mikelsaar Short Communications Pages: 217 - 220
Untersuchungen zum Polymorphismus der Galaktose-1-Phosphat-Uridyltransferase (EC: 2.7.7.12) mittels Agarosegelelektrophorese P. KühnlL. NowickiW. Spielmann Kurze Originalmitteilungen Pages: 227 - 230
Transferrin polymorphism in Central Thailand H. H. DahmW. SchlootH. W. Goedde Short Communications Pages: 231 - 233
Malformative syndrome with ring chromosome 13 J. P. FrynsJ. DerooverE. Lebas Clinical Case Reports Pages: 235 - 240
Partial trisomy 8: Trisomy of the distal part of the long arm of chromosome number 8+(8q2) in a severely retarded and malformed girl J. P. FrynsH. VerresenJ. J. Cassiman Clinical Case Reports Pages: 241 - 246
Trisomy 12p due to familial t(12p-,6q+) translocation J. P. FrynsH. Van den BergheJ. J. Cassiman Clinical Case Reports Pages: 247 - 252
Hereditary malignant hyperpyrexia associated with muscle adenylate kinase deficiency J. SchmittK. SchmidtH. Ritter Clinical Case Reports Pages: 253 - 257
A triploid human abortus due to dispermy Norio NiikawaTadashi Kajii Clinical Case Reports Pages: 261 - 264
