Cytological findings of 10 cases with i(Xq) and one with dic(X)(qter→cen→p22:: p11→qte) Hiroko FujitaYoko TanigawaYoshiaki Okada Original Investigations Pages: 147 - 155
Likely linkage: Inv with Jk B. J. B. KeatsN. E. MortonD. C. Rao Original Investigations Pages: 157 - 159
Study of the human male meiosis M. L. De TorresJ. A. Abrisqueta Original Investigations Pages: 161 - 168
Quantitative analysis of C-bands based on optical density profiles in human chromosomes V. A. BenyushV. G. LuckashA. V. Shtannikov Original Investigations Pages: 169 - 175
Replication bypass model of sister chromatid exchanges and implications for Bloom's Syndrome and Fanconi's anemia David A. Shafer Original Investigations Pages: 177 - 190
Three rare G-6-PD variants from Porto Alegre, Brazil Mara H. HutzA. YoshidaF. M. Salzano Original Investigations Pages: 191 - 197
Gm and Km(Inv) frequencies in two Roumanian populations Walter E. JohnsonPeter H. KohnArthur G. Steinberg Original Investigations Pages: 199 - 211
Variable composition of X chromosomal mosaics: Due to asynchronous cell division during early embryogenesis? Hans-Hilger RopersTiemo Grimm Short Communications Pages: 213 - 215
Chromosome banding study of the Cornelia de Lange syndrome J. R. MerikangasK. MerikangasS. Pan Short Communications Pages: 217 - 219
Grandmaternal age at birth of parents of children with trisomy 21 Z. PappÉ. VáradiZ. Szabó Short Communications Pages: 221 - 224
Serum Gc system in liver cirrhosis and hepatoma George TheodoropoulosGerasimos RigatosKimon Melissinos Short Communications Pages: 225 - 228
A case of chronic myeloid leukemia with a translocation (12;22)(p13;q11) M. van der Blij-PhilipsenW. P. M. BreedT. W. J. Hustinx Clinical Case Reports Pages: 229 - 231
Interstitial deletion of the long arm of chromosome 2 in a polymalformed newborn-karyotype: 46,XX,del(2)(q21;q24) J. P. FrynsB. Van BosstraetenH. Van den Berghe Clinical Case Reports Pages: 233 - 238
Pericentric inversion and partial monosomy 4q associated with congenital anomalies Françoise ServilleA. Broustet Clinical Case Reports Pages: 239 - 242
18p- Syndrome resulting from 14q/18q ‘dicentric’ fusion translocation Steve J. FunderburkRobert S. SparkesIvana Klisak Clinical Case Reports Pages: 243 - 250
Human triploid embryo J. del MazoM. A. Martinez GonzálezJ. A. Abrisqueta Clinical Case Reports Pages: 251 - 256
Scientific method and the Philadelphia chromosome Peter H. Fitzgerald Letters to the Editors Pages: 257 - 259