Kartagener's syndrome and the syndrome of immotile cilia H. -D. Rott Review Articles Pages: 249 - 261
Trisomy for the distal third of the long arm of chromosome 19 in brother and sister W. Schmid Original Investigations Pages: 263 - 270
‘Complete’ trisomy 5p; de novo translocation t(2;5)(q36;p11) with isochromosome 5p N. J. LeschotK. S. Lim Original Investigations Pages: 271 - 278
Trisomy 6q25→6qter in a severely retarded 7-year-old boy with turricephaly, bow-shaped mouth, hypogenitalism and club feet W. SchmidV. D'ApuzzoE. Rossi Original Investigations Pages: 279 - 284
Origin of trisomies in human spontaneous abortions Terry HassoldAileen Matsuyama Original Investigations Pages: 285 - 294
Three cases of sex chromosome mosaicism with a nonfluorescent Y K. MadanL. GoorenJ. Schoemaker Original Investigations Pages: 295 - 304
Congenital glaucoma: Genetic models Florence DemenaisCatherine BonaïtiJean Frézal Original Investigations Pages: 305 - 317
Evidence for a Null allele at the Esterase D (EC 3.1.1.1) locus R. S. SparkesS. TargumM. Crist Original Investigations Pages: 319 - 323
Heterozygote manifestation in recessive generalized myotonia P. E. Becker Short Communications Pages: 325 - 329
Frequency of sister chromatid exchanges in Bloom syndrome fibroblasts reduced by cocultivation with normal cells C. R. BartramH. W. RüdigerE. Passarge Short Communications Pages: 331 - 334
Trisomy 8p due to the 3:1 segregation of the balanced translocation t(8;15)mat G. I. LazjukI. W. LurieM. K. Nedzved Clinical Case Reports Pages: 335 - 339
Partial trisomy 18q12, due to intrachromosomal duplication, is not associated with typical 18 trisomy phenotype J. P. FrynsL. VinkenH. Van den Berghe Clinical Case Reports Pages: 341 - 344
Pure red cell hypoplasia associated with long-arm deletion of chromosome 5 Joseph DiBenedetto JrTeresita Padre-MendozaMaurice M. Albala Clinical Case Reports Pages: 345 - 348
Šereševskij-Turner's syndrome or Turner's syndrome? G. R. Fraser Letters to the Editors Pages: 353 - 353