Paracentric inversion in the short arm of chromosome 1 J. DerooverJ. P. FrynsH. Van Den Berghe Original Investigations Pages: 117 - 121
Partial duplication of 17p Margret Bartsch-SandhoffGertrud Hieronimi Original Investigations Pages: 123 - 127
Complete deficiency of constitutive heterochromatin on a human chromosome 9 C. H. C. M. BuysJ. M. M. YpmaW. L. Gouw Original Investigations Pages: 129 - 132
Computer-aided analysis of chromosomal aberrations occurring in an abnormal human karyotype S. HazoutA. M. VenuatC. Rosenfeld Original Investigations Pages: 133 - 145
Chromosome distribution studies after inorganic lead exposure L. VerschaeveM. DriesenC. Susanne Original Investigations Pages: 147 - 158
Linkage studies on the human Pi, Gm, GLO, and HLA genes K. BenderC. R. MüllerT. F. Wienker Original Investigations Pages: 159 - 166
Possible trisomy 1q25→1q32 in a malformed girl with a de novo insertion in 1q A. Schinzel Original Investigations Pages: 167 - 173
Tertiary trisomy 14q-, due to paternal balanced translocation 46,XY,t(1;14)(q44;q22) Gy. KovacsClara Mihai Original Investigations Pages: 175 - 178
Partial trisomy 4q in two unrelated cases Milly AndrleA. ErlachA. Rett Original Investigations Pages: 179 - 183
Quantitative studies on the arrangement of human metaphase chromosomes H. ZanklD. MichaelsenK. D. Zang Original Investigations Pages: 185 - 189
Partial mispairing and crossing-over between β0 and δ genes as the origin of the δ β0 thalassemia gene J. M. CantúB. IbarraJ. Sánchez-Corona Original Investigations Pages: 191 - 198
Karyotype instability with multiple 7/14 and 7/7 rearrangements T. W. J. HustinxJ. M. J. C. ScheresA. H. Janssen Original Investigations Pages: 199 - 208
Human lymphocyte cell cycle: Studies with the use of BrUdR P. Auf der MaurKristina Berlincourt-Böhni Original Investigations Pages: 209 - 215
Congenital scalp defects associated with postaxial polydactyly J. P. FrynsH. Van den Berghe Original Investigations Pages: 217 - 219
Triplex gene dosage effect of TPI and G3PD in a human lymphoblastoid cell line with partial trisomy 12p13 and 18p C. JunienJ. C. KaplanG. Lenoir Short Communications Pages: 221 - 223
Translocation between chromosome 7 and chromosome 22, t(7;22)(p22;q12), in a patient with chronic myelocytic leukemia Gösta GahrtonKristina FribergLore Zech Clinical Case Reports Pages: 225 - 227
Partial trisomy 16q resulting from maternal translocation P. BalestrazziG. GiovannelliB. Dallapiccola Clinical Case Reports Pages: 229 - 235
Isodicentric X chromosome in a woman with characteristics of gonadal dysgenesis Živana LaćaMarklena IvanovićSlavka Morić-Petrović Clinical Case Reports Pages: 237 - 241