Prospects for homologous recombination in human gene therapy Manuel A. Vega Review Article Pages: 245 - 253
Induction of distamycin A-inducible rare fragile sites and increased sister chromatid exchanges at the fragile site Hideo TsujiAkitsu HitomiTada-aki Hori Original Investigations Pages: 254 - 260
Non-isotopic detection of chromosome 1 in human meiosis and demonstration of disomic sperm nuclei Martina GuttenbachMichael Schmid Original Investigations Pages: 261 - 265
High prevalence of aspartylglycosaminuria among school-age children in eastern Finland Tarja MononenIlkka MononenEila Airaksinen Original Investigations Pages: 266 - 268
Molecular characterization of a patient with del(1)(q23–q25) Brunella FrancoLi-Wen LaiJames R. Lupski Original Investigations Pages: 269 - 277
The murine Rb(6.16) translocation: evidence for sperm selection and a modulating effect of aging Ivar P. AranhaPatricia A. Martin-DeLeon Original Investigations Pages: 278 - 284
Cytogenetic investigations in three cell types of a Saudi family with ataxia telangiectasia Manjula WaghrayGeneroso G. GasconMohammed A. Hannan Original Investigations Pages: 285 - 289
Characterization of seven DA/DAPI-positive bisatellited marker chromosomes by in situ hybridization Rina PlattnerNyla A. HeeremaCatherine G. Palmer Original Investigations Pages: 290 - 296
Dominant mutations in familial lethal and severe osteogenesis imperfecta Lola Cohen-SolalJacky BonaventurePierre Maroteaux Original Investigations Pages: 297 - 301
Sister chromatid exchanges are preferentially induced at expressed and nonexpressed common fragile sites Betsy Hirsch Original Investigations Pages: 302 - 306
Detection of human spermatid-specific transcripts in peripheral blood lymphocytes of males and females Ryszard SlomskiManfred SchloesserWolfgang Engel Original Investigations Pages: 307 - 310
Dopamine beta-hydroxylase gene excluded in four subtypes of hereditary dystonia Deborah SchubackPatricia KramerXandra O. Breakefield Original Investigations Pages: 311 - 316
Recurrent ctb(7)(q31.3) and possible laminin involvement in a neonatal cutis laxa with a Marfan phenotype D. BonneauJ. L. HuretM. Larrègue Original Investigations Pages: 317 - 319
Inherited ring chromosomes: an analysis of published cases György KosztolányiKároly MéhesErnest B. Hook Original Investigations Pages: 320 - 324
Assignment of the gene coding for human cytochrome c oxidase subunit VIb to chromosome 19, band q13.1, by fluorescence in situ hybridisation Jan-Willem TaanmanAnneke Y. van der VeenCharles H. C. M. Buys Original Investigations Pages: 325 - 327
Three unique base pair changes in a family with Gaucher disease Nurit EyalNurit FironMia Horowitz Original Investigations Pages: 328 - 332
T296→M, a common mutation causing mild hemophilia B in the Amish and others: founder effect, variability in factor IX activity assays, and rapid carrier detection Rhett P. KetterlingCynthia D. K. BottemaSteve S. Sommer Original Investigations Pages: 333 - 337
X-linked anhidrotic ectodermal dysplasia and de novo t(X;1) in a female Janusz LimonJadwiga FilipiukJadwiga Roszkiewicz Original Investigations Pages: 338 - 340
Increased band sharing in DNA fingerprints of an inbred human population R. J. BellamyC. F. InglehearnS. S. Bhattacharya Original Investigations Pages: 341 - 347
Choroideremia: linkage analysis with physically mapped close DNA-markers Eeva-Marja SankilaPertti SistonenAlbert de la Chapelle Original Investigations Pages: 348 - 352
Genotype-phenotype correlation and germline mosaicism in DMD/BMD patients with deletions of the dystrophin gene A. E. CovoneM. LeroneG. Romeo Original Investigations Pages: 353 - 360
Extended MHC haplotypes and CYP21/C4 gene organisation in Irish 21-hydroxylase deficiency families Paul J. SinnottColm CostiganTom Strachan Original Investigations Pages: 361 - 366
Human platelet basic protein/connective tissue activating peptide-III maps in a gene cluster on chromosome 4q12–q13 along with other genes of the β-thromboglobulin superfamily R. H. WengerH. HameisterK. J. Clemetson Short Communications Pages: 367 - 368
New distal marker closely linked to the fragile X locus T. J. M. HulsebosB. A. OostraA. Westerveld Short Communications Pages: 369 - 372
Recurrent mutation at aa 792 in the LDL receptor gene in a French patient N. LouxP. BenlianC. Junien Short Communications Pages: 373 - 375
Human polymorphic probe pE1.8 detects SacI polymorphism in the ribonucleotide reductase M1 subunit gene Jennifer ByrnePeter Smith OriginalPaper Pages: 376 - 376