Genetics of the human electroencephalogram (EEG) and event-related brain potentials (ERPs): a review C. E. M. van BeijsterveldtD. I. Boomsma Review Article Pages: 319 - 330
Molecular analysis of aniridia patients for deletions involving the Wilms' tumor gene M. DrechslerE. J. Meijers-HeijboerB. Royer-Pokora Original Investigation Pages: 331 - 338
Identification, characterisation and clinical applications of cosmids from the telomeric and centromeric regions of the long arm of chromosome 22 Ya-Gang XieFei-Yu HanMagnus Nordenskjöld Original Investigation Pages: 339 - 345
A polymorphic alpha satellite sequence specific for human chromosome 13 detected by oligonucleotide primed in situ labelling (PRINS) Franck PellestorAnne GirardetJean-Paul Charlieu Original Investigation Pages: 346 - 348
Distinct RB1 gene mutations with low penetrance in hereditary retinoblastoma Dietmar R. LohmannBirgit BrandtBernhard Horsthemke Original Investigation Pages: 349 - 354
Chromosome 14 maternal uniparental disomy in the euploid cell line of a fetus with mosaic 46,XX/47,XX,+14 karyotype Silvia Maria SirchiaChiara De AndreisGiuseppe Simoni Original Investigation Pages: 355 - 358
Biochemical and molecular studies of 132 patients with galactosemia Won G. NgYan-Kang XuJuergen K. V. Reichardt Original Investigation Pages: 359 - 363
No evidence for linkage of long QT syndrome and chromosome 11p15.5 markers in a Chinese family: evidence for genetic heterogeneity Yu-Lin KoShih-Ann ChenCheng-Wen Wu Original Investigation Pages: 364 - 366
Chromosome 4q35 haplotypes and DNA rearrangements segregating in affected subjects of 19 Italian families with facioscapulohumeral musculatur dystrophy (FSHD) S. CacurriG. DeiddaL. Felicetti Original Investigation Pages: 367 - 374
Polymorphisms of the prion protein gene in Italian patients with Creutzfeldt-Jakob disease Mirella SalvatoreMaurizio GenuardiMaurizio Pocchiari Original Investigation Pages: 375 - 379
Genetic linkage analyses of Romano-Ward syndrome (RWS) in 13 Japanese families Toshihiro TanakaKen-ichi NakaharaYusuke Nakamura Original Investigation Pages: 380 - 384
β-Thalassemia mutations in Singapore — a strategy for prenatal diagnosis Ivy S. L. NgJoyce B. K. OngHai Yang Law Original Investigation Pages: 385 - 388
A fluorescent in situ hybridization analysis of X chromosome pairing in early human female meiosis Edith Y. ChengStanley M. Garder Original Investigation Pages: 389 - 394
Molecular analysis of the (CGG)n expansion in the FMR-1 gene in 59 Spanish fragile X syndrome families M. MilàH. KruyerX. Estivill Original Investigation Pages: 395 - 400
DNA haplotype-dependent differences in the amino acid sequence of debrisoquine 4-hydroxylase (CYP2D6): evidence for two major allozymes in extensive metabolisers S. PanseratC. MuraR. Krishnamoorthy Original Investigation Pages: 401 - 406
Interleukin 1 receptor antagonist gene polymorphism association with lichen sclerosus Frances E. ClayMichael J. CorkGordon W. Duff Original Investigation Pages: 407 - 410
Nondisjunction of human acrocentric chromosomes: studies of 432 trisomic fetuses and liveborns Michael V. ZaragozaPatricia A. JacobsTerry Hassold Original Investigation Pages: 411 - 417
Linkage mapping of the tumor necrosis factor receptor 2 (TNFR2) gene to 1p36.2 using the single-strand conformation polymorphism technique Bruce A. KaufmanPeter S. WhiteGarrett M. Brodeur Original Investigation Pages: 418 - 422
Parental origin of the extra chromosomes in polysomy X C. A. LealJohn W. BelmontC. Medina Original Investigation Pages: 423 - 426
Fine mapping of human PI 3-kinase associated p85α transcripts in the YAC contig surrounding the spinal muscular atrophy gene Jana HuschenbettAlexander GaschAstrid Speer Original Investigation Pages: 427 - 431
Genetic analysis of Cuban autosomal dominant polycystic kidney disease kindreds using RFLPs and microsatellite polymorphisms linked to the PKD1 locus Miguel ViribayRaúl FerreiraJosé L. San Millan Original Investigation Pages: 432 - 436
Refined localization of TSC1 by combined analysis of 9q34 and 16pl3 data in 14 tuberous sclerosis families Bart JanssenJulian SampsonDicky Halley Short Communication Pages: 437 - 440
Two novel point mutations in the cytochrome b 558 heavy chain gene, detected in two Japanese patients with X-linked chronic granulomatous disease Tadashi ArigaYukio SakiyamaShuzo Matsumoto Short Communication Pages: 441 - 441
Refined mapping of the human Ets-related gene Elk-1 to Xp11.2–p11.4, distal to the OATL1 region Martin JanzUlrich LehmannAlfred Nordheim Short Communication Pages: 442 - 444
Etiological aspects of congenital diaphragmatic hernia: results of a case comparison study Albert P. BosAnnemieke M. PattenierJan C. Molenaar Short Communication Pages: 445 - 446
Characterisation of a 5-bp deletion in exon 4 of the factor VIII gene: concordance with slipped-mispairing at DNA replication Sanjay I. BidichandaniW. George LanyonJ. Michael Connor Short Communication Pages: 447 - 449
Characterization of several DNA polymorphic markers in the LIF gene region A. Moreau-AubryM. T. AndreJ. P. Moisan OriginalPaper Pages: 450 - 451
Polymorphism in the human E-selectin gene detected by PCR-SSCP Katrin WenzelRita HankeAstrid Speer OriginalPaper Pages: 452 - 453
A PvuII polymorphism near exon 2 of the dystrophin gene Gareth S. CrossJohn T. DonnellyAbid L. Sharif OriginalPaper Pages: 454 - 455
