A family with whistling-face-syndrome Angelika WettsteinG. BuchingerU. Banniza v. Bazan Original Investigations Pages: 177 - 189
Partial trisomie 5q: Three different phenotypes depending on different duplication segments A. RodewaldMerve ZanklK. D. Zang Original Investigations Pages: 191 - 198
The offspring of marriage between two first cousins with the same reciprocal translocation t(2;7)(p11;q31) G. SimoniL. DalpràM. G. Tibiletti Original Investigations Pages: 199 - 202
Recurrence risks for down syndrome Tamara June ListerO. Frota-Pessoa Original Investigations Pages: 203 - 208
Reciprocal translocations: A way to predict the mode of imbalanced segregation by pachytene-diagram drawing P. JalbertB. SeleH. Jalbert Original Investigations Pages: 209 - 222
Suppression of spontaneous and mitomycin C-induced chromosome aberrations in Fanconi's anemia by cell fusion with normal human fibroblasts M. C. Yoshida Original Investigations Pages: 223 - 226
Activity of rRNA genes in cells of a patient with Down syndrome mosaic R. -D. WegnerP. AldenhoffK. Sperling Original Investigations Pages: 227 - 229
Bipolar manic-depressive psychoses: Results of a genetic investigation J. AngstR. FreyE. Zerbin-Rüdin Original Investigations Pages: 237 - 254
Regional assignment of a 2.1-kb repetitive sequence to the distal part of the human Y heterochromatin J. SchmidtkeM. Schmid Original Investigations Pages: 255 - 257
5-Bromodeoxycytidine in the study of sister chromatid exchanges in human lymphocytes A. F. ZakharovT. L. Bairamjan Original Investigations Pages: 259 - 263
Chromosome heteromorphisms in the Japanese Toshio SofuniKazumi TanabeAkio A. Awa Original Investigations Pages: 265 - 270
A girl with the Prader-Willi Syndrome and Robertsonian translocation 45,XX,t(14;15)(p11;q11) which was present in three normal family members Arabella SmithMichael Noel Clinical Case Reports Pages: 271 - 273
Diaphragmatic defects in children of consanguineous parents Ilan AradGraciela C. LijovetzkyTirza Cohen Clinical Case Reports Pages: 275 - 277
