1. Kartagener's syndrome and the syndrome of immotile cilia

   • H. -D. Rott

   Review Articles Pages: 249 - 261

2. Trisomy for the distal third of the long arm of chromosome 19 in brother and sister

   • W. Schmid

   Original Investigations Pages: 263 - 270

3. ‘Complete’ trisomy 5p; de novo translocation t(2;5)(q36;p11) with isochromosome 5p

   • N. J. Leschot
   • K. S. Lim

   Original Investigations Pages: 271 - 278

4. Trisomy 6q25→6qter in a severely retarded 7-year-old boy with turricephaly, bow-shaped mouth, hypogenitalism and club feet

   • W. Schmid
   • V. D'Apuzzo
   • E. Rossi

   Original Investigations Pages: 279 - 284

5. Origin of trisomies in human spontaneous abortions

   • Terry Hassold
   • Aileen Matsuyama

   Original Investigations Pages: 285 - 294

6. Three cases of sex chromosome mosaicism with a nonfluorescent Y

   • K. Madan
   • L. Gooren
   • J. Schoemaker

   Original Investigations Pages: 295 - 304

7. Congenital glaucoma: Genetic models

   • Florence Demenais
   • Catherine Bonaïti
   • Jean Frézal

   Original Investigations Pages: 305 - 317

8. Evidence for a Null allele at the Esterase D (EC 3.1.1.1) locus

   • R. S. Sparkes
   • S. Targum
   • M. Crist

   Original Investigations Pages: 319 - 323

9. Heterozygote manifestation in recessive generalized myotonia

   • P. E. Becker

   Short Communications Pages: 325 - 329

10. Frequency of sister chromatid exchanges in Bloom syndrome fibroblasts reduced by cocultivation with normal cells

    • C. R. Bartram
    • H. W. Rüdiger
    • E. Passarge

    Short Communications Pages: 331 - 334

11. Trisomy 8p due to the 3:1 segregation of the balanced translocation t(8;15)mat

    • G. I. Lazjuk
    • I. W. Lurie
    • M. K. Nedzved

    Clinical Case Reports Pages: 335 - 339

12. Partial trisomy 18q12, due to intrachromosomal duplication, is not associated with typical 18 trisomy phenotype

    • J. P. Fryns
    • L. Vinken
    • H. Van den Berghe

    Clinical Case Reports Pages: 341 - 344

13. Pure red cell hypoplasia associated with long-arm deletion of chromosome 5

    • Joseph DiBenedetto Jr
    • Teresita Padre-Mendoza
    • Maurice M. Albala

    Clinical Case Reports Pages: 345 - 348

14. Clinical consequence of Xp-

    • J. J. Hoo

    Letters to the Editors Pages: 349 - 351

15. Šereševskij-Turner's syndrome or Turner's syndrome?

    • G. R. Fraser

    Letters to the Editors Pages: 353 - 353