Isolation of anonymous, polymorphic DNA fragments from human chromosome 22q12-qter Jan P. DumanskiAd H. M. Geurts van KesselMagnus Nordenskjöld Original Investigations Pages: 219 - 222
Identification of complex DNA polymorphisms based on variable number of tandem repeats (VNTR) and restriction site polymorphism John S. WayeRon M. Fourney Original Investigations Pages: 223 - 227
Rapid detection of deletions in the Duchenne muscular dystrophy gene by PCR amplification of deletion-prone exon sequences M. HentemannJ. ReissD. N. Cooper Original Investigations Pages: 228 - 232
Marfan syndrome: exclusion of genetic linkage to five genes coding for connective tissue components in the long arm of chromosome 2 Katariina KainulainenAslak SavolainenLeena Peltonen Original Investigations Pages: 233 - 236
Demonstration of chromosome replication by BrdU antibody technique and electron microscopy W. VogelK. MehnertS. Pentz Original Investigations Pages: 237 - 240
Haplotyping of the human porphobilinogen deaminase gene in acute intermittent porphyria by polymerase chain reaction Jin-Sung LeeJan LindstenMaria Anvret Original Investigations Pages: 241 - 243
Nucleolus organizer regions in human lymphocytes as studied with premature chromosome condensation Franz WachtlerChrista RoubicekHans Georg Schwarzacher Original Investigations Pages: 244 - 248
Increased frequency of 6-thioguanine-resistant peripheral blood lymphocytes in Werner syndrome patients Ken-ichiro FukuchiKiyoji TanakaRaymond J. Monnat Jr. Original Investigations Pages: 249 - 252
A panel of restriction fragment length polymorphisms for chromosomal band 11p13 Vicki HuffDuane A. ComptonGrady F. Saunders Original Investigations Pages: 253 - 257
Cell kinetic disturbances induced by treatment of human diploid fibroblasts with 5-azacytidine indicate a major role for DNA methylation in the regulation of the chromosome cycle Martin PootJulia KoehlerJean H. Priest Original Investigations Pages: 258 - 262
New informative polymorphism at the DXS304 locus, a close distal marker for the fragile X locus F. RousseauA. VincentJ. L. Mandel Original Investigations Pages: 263 - 266
Marker haplotype association with growth in German cystic fibrosis patients Burkhard TümmlerAntje AschendorffJoachim Hundrieser Original Investigations Pages: 267 - 273
Analysis of the transgenome of MET transfectant cell lines reveals that MET activation is accompanied by an interstitial insertion Peter J. ScamblerBrandon WainwrightColin Cooper Original Investigations Pages: 274 - 278
Extensive sequence polymorphisms associated with chromosome 10 alpha satellite DNA and its close linkage to markers from the pericentromeric region Jingshi WuKenneth K. Kidd Original Investigations Pages: 279 - 282
An informative polymorphism detectable by polymerase chain reaction at the 3′ end of the dystrophin gene C. OudetR. HeiligJ. L. Mandel Short Communications Pages: 283 - 285
Probe, VK5B, is located in the same interval as the autosomal dominant adult polycystic kidney disease locus, PKD1 V. J. HylandG. K. SuthersG. R. Sutherland Short Communications Pages: 286 - 288
Maternal meiosis II nondisjunction in a case of 47,XXY testicular feminization Ulrich MüllerNancy R. SchneiderGolder N. Wilson Short Communications Pages: 289 - 292
Human pepsinogen A (PGA): an informative gene complex located at 11q13 Farzin H. BoudiRagnhild A. LotheR. Thomas Taggart Short Communications Pages: 293 - 295
Growth retardation in Wolf-Hirschhorn syndrome Atsuko FujimotoMiriam G. Wilson Clinical Case Reports Pages: 296 - 297
Trisomy 18 mosaicism in an adult woman with normal intelligence and history of miscarriage E. GersdorfB. UtermannG. Utermann Clinical Case Reports Pages: 298 - 299
