Isolation of DNA sequences on human chromosome 21 by application of a recombination-based assay to DNA from flow-sorted chromosomes Umadevi TantravahiGordon D. StewartSamuel A. Latt Original Investigations Pages: 196 - 202
Three major cytogenetic subgroups can be identified among chromosomally abnormal solitary lipomas Nils MandahlSverre HeimFelix Mitelman Original Investigations Pages: 203 - 208
Polymorphism of MHC class III genes: definition of restriction fragment linkage groups and evidence for frequent deletions and duplications N. GhanemB. Uring-LambertG. Lefranc Original Investigations Pages: 209 - 218
Linkage analysis using multiple DNA polymorphic markers in normal families and in families with fragile X syndrome S. N. ThibodeauH. R. DorkinsK. E. Davies Original Investigations Pages: 219 - 227
Analysis for linkage between F13A and three chromosome 6 marker loci: evidence for 6pter: F13A:HLA:GL01:cen gene order P. WongL. KomarnickiP. J. McAlpine Original Investigations Pages: 228 - 230
Spermatogenesis in two patients with the fragile X syndrome R. JohannissonU. Froster-IskeniusM. A. Hulten Original Investigations Pages: 231 - 234
cDNA cloning, expression and mapping of human laminin B2 gene to chromosome 1q31 Marie-Geneviève MatteiDominique WeilMon-Li Chu Original Investigations Pages: 235 - 241
Effect of caffeine in Fanconi anemia Laure SabatierBernard Dutrillaux Original Investigations Pages: 242 - 244
Type I procollagen in the severe non-lethal form of osteogenesis imperfecta Ruggero TenniGiuseppe CettaAlessandro A. Castellani Original Investigations Pages: 245 - 250
A recombinant X chromosome in a short statured girl resulting from a maternal pericentric inversion D. P. DuckettI. D. Young Original Investigations Pages: 251 - 254
Comparison between the allelic frequency distribution of the Ha-ras 1 locus in normal individuals and patients with lymphoma, breast, and ovarian cancer B. CorellB. Zoll Original Investigations Pages: 255 - 259
The human tyrosine aminotransferase gene: characterization of restriction fragment length polymorphisms and haplotype analysis in a family with tyrosinemia type II Eva-Maria WestphalErnst NattGerd Scherer Original Investigations Pages: 260 - 264
Human satellite-III DNA: an example of a “macrosatellite” polymorphism C. FowlerR. DrinkwaterL. Burgoyne Original Investigations Pages: 265 - 272
A complete deletion of the factor IX gene and new TaqI variant in a hemophilia B kindred S. A. M. TaylorD. P. LillicrapB. N. White Original Investigations Pages: 273 - 276
Restriction fragment length polymorphisms detected by anonymous DNA probes mapped to defined intervals of human chromosome 16 V. J. HylandS. GristG. R. Sutherland Original Investigations Pages: 277 - 279
Molecular analysis of a reciprocal translocation t(5;11)(q11;p13) in a WAGR patient Hugues PuissantMartine AzoulayClaudine Junien Original Investigations Pages: 280 - 282
Regional chromosomal localisation of APOA2 to 1q21–1q23 H. R. Middleton-PriceJ. A. van den BergheS. Malcolm Original Investigations Pages: 283 - 285
Increased amounts of small polydisperse circular DNA (spcDNA) in angiofibroma-derived cell cultures from patients with tuberous sclerosis (TS) C. NeidlingerG. AssumG. Klotz Short Communications Pages: 286 - 288
Linkage between the variegate porphyria (VP) and the alpha-1-antitrypsin (PI) genes on human chromosome 14 S. BissbortH. W. HitzerothK. Bender Short Communications Pages: 289 - 290