Pure trisomy 17p in 60% of cells F. ShabtaiA. ShalevE. Elian Original Investigations Pages: 263 - 268
Interstitial deletion 13q syndromes: A report on two unrelated patients M. Serena-LungarottiAnna CalabroB. Dallapiccola Original Investigations Pages: 269 - 274
An uncommon phenotypical variant in the Shereshevsky-Turner syndrome I. G. DzenisN. N. Antipina Original Investigations Pages: 275 - 279
Sister chromatid exchanges in cultured peripheral lymphocytes from twins C. PedersenEva OláhU. Merrild Original Investigations Pages: 281 - 294
Nucleolar organizers in human oocytes at meiotic prophase I, studied by the silver-NOR method and electron microscopy M. HartungC. MirreA. Stahl Original Investigations Pages: 295 - 308
Mutagenic effects of isonicotinic acid hydracide in Fanconi's anemia Traute M. SchroederChristine Stahl-Maugé Original Investigations Pages: 309 - 321
On the nature of sickle-cell disease in the Arabian Peninsula M. A. F. El-Hazmi Original Investigations Pages: 323 - 335
Calculating genetic risk figures using a programmable pocket calculator G. R. Stalder Original Investigations Pages: 337 - 341
Frequency of sister chromatid exchanges in cigarette smokers P. Bala Krishna Murthy Short Communications Pages: 343 - 345
Partial deficiency of red cell 6-phosphogluconate dehydrogenase: A family study F. AjmarG. LamedicaA. Campostano Short Communications Pages: 347 - 351
