Human mitochondrial DNA types in Finland Johanna VilkkiMarja-Liisa SavontausEeva K. Nikoskelainen Original Investigations Pages: 317 - 321
Similar molecular deletions on chromosome 15q11.2 are encountered in both the Prader-Willi and Angelman syndromes T. A. Donlon Original Investigations Pages: 322 - 328
Galactosialidosis: molecular heterogeneity in biosynthesis and processing of protective protein for β-galactosidase Eiji NanbaAkihiko TsujiYoshiyuki Suzuki Original Investigations Pages: 329 - 332
Blastomere karyotyping and transfer of chromosomally selected embryos C. BacchusW. Buselmaier Original Investigations Pages: 333 - 336
The gene for X-linked progressive mixed deafness with perilymphatic gusher during stapes surgery (DFN3) is linked to PGK Han G. BrunnerCor A. van BennekomHans-Hilger Ropers Original Investigations Pages: 337 - 340
Familial amyloidotic polyneuropathy: transthyretin (prealbumin) variants in kindreds of Italian origin Maria João Mascarenhas SaraivaPedro P. CostaFabrizio Salvi Original Investigations Pages: 341 - 343
Population cytogenetics of folate-sensitive fragile sites Marketta Kähkönen Original Investigations Pages: 344 - 348
The pathology of trisomy 13 syndrome Philippe MoermanJean-Piere FrynsJoseph Lauweryns Original Investigations Pages: 349 - 356
Cytogenetic analysis of sperm from a male heterozygous for a 13;14 Robertsonian translocation Renee H. Martin Original Investigations Pages: 357 - 361
Use of restriction fragment length polymorphic probes in the analysis of Down's syndrome trisomy A. M. Millington-WardP. L. Pearson Original Investigations Pages: 362 - 370
A new LDL receptor gene deletion mutation in the South African population Howard E. HendersonG. Michael B. BergerA. David Marais Original Investigations Pages: 371 - 374
Dissociation between mental retardation and fragile site expression in a family with fragile X-linked mental retardation M. A. VoelckelM. G. MatteiJ. F. Mattei Original Investigations Pages: 375 - 378
Segregation of linked probes to myotonic dystrophy in a family demonstrating that 152 and APOC2 are on the same side of DM on 19q K. JohnsonE. NimmoR. Williamson Original Investigations Pages: 379 - 381
Synergistic effect of hydroxyurea and excessive thymidine on the expression of the common fragile sites at 3p14 and 16q23 Zu-an YanXinzhi LiXianting Zhou Original Investigations Pages: 382 - 384
Glucose-6-phosphate dehydrogenase variants and their frequency in Guangdong, China C. S. DuY. K. XuL. B. Liu Original Investigations Pages: 385 - 388
Assignment of human platelet GP2B (GPIIb) gene to chromosome 17, region q21.1-q21.3 Nguyen van CongG. UzanJ. Frézal Original Investigations Pages: 389 - 392
Pelizaeus-Merzbacher disease: identification of heterozygotes with magnetic resonance imaging? Eugen BoltshauserAlbert SchinzelAnton Valavanis Short Communications Pages: 393 - 394
Lysinuric protein intolerance mutation is not expressed in the plasma membrane of erythrocytes D. W. SmithC. R. ScriverO. Simell Short Communications Pages: 395 - 396
Assignment of human coagulation factor XII (fXII) to chromosome 5 by cDNA hybridization to DNA from somatic cell hybrids F. CitarellaM. TripodiM. Rocchi Short Communications Pages: 397 - 398
Different numbers of maternal and paternal siblings of cystic fibrosis patients Jürgen GedscholdReinhard SziborMargot Berger Short Communications Pages: 399 - 400
Interstitial deletion of chromosome 15: two cases L. de F. FormigaL. PoenaruM. Pierson Clinical Case Report Pages: 401 - 404
