Structural variability of human chromosome 9 in relation to its evolution I. Hansmann Original Investigations Pages: 247 - 262
Karyotyp-Phenotyp-Lorrelation bei einem 46,Xdel(X)(p22)-Befund M. Bartsch-SandhoffR. TerindeW. Scholz Original Investigations Pages: 263 - 270
47,+(9q-) in unrelated three children with plasma growth hormon deficiency Hiroko FujitaMotoko ShimazakiToshiaki Oura Original Investigations Pages: 271 - 282
Banding pattern observed in human chromosomes by the modified BSG technique N. Kanda Original Investigations Pages: 283 - 292
Q-banding of human chromosomes after BUdR and BCdR treatment Erica M. BühlerTaiso TsuchimotoL. Pia Jurik Original Investigations Pages: 309 - 314
Chromosome analysis on 930 consecutive newborn children using quinacrine fluorescent banding technique C. C. LinM. M. GedeonL. M. Sewell Original Investigations Pages: 315 - 328
Serum immunoglobulin M, G, and A concentration levels in Turner's syndrome compared with normal women and men Knud JensenPer Hyltoft PetersenJohannes Nielsen Original Investigations Pages: 329 - 334
Biochemical characteristics of collagen produced by long term cultivated amniotic fluid cells J. HurychM. MacekD. Řezáčová Original Investigations Pages: 335 - 340
Possible assignment of the glyoxalase I (GLO) gene to chromosome 6 using man-mouse somatic cell hybrids K. BenderK. -H. Grzeschik Short Communications Pages: 341 - 345
The trisomy 18 syndrome with an E/G translocation Danuta DziekanowskaP. DziubaT. Sobański Clinical Case Reports Pages: 347 - 349
A female infant with monosomy 21 P. DziubaD. DziekanowskaH. Hübner Clinical Case Reports Pages: 351 - 353
9p trisomy identified by Giemsa-11 Herman E. WyandtFrederick HechtGerald Prescott Clinical Case Reports Pages: 355 - 358