Multicolor fluorescence in situ hybridization on metaphase chromosomes and interphase Halo-preparations using cosmid and YAC clones for the simultaneous high resolution mapping of deletions in the dystrophin gene Chintana TocharoentanapholMarion CremerThomas Ried Original Investigations Pages: 229 - 235
A large family with features of pseudoachondroplasia and multiple epiphyseal dysplasia: exclusion of seven candidate gene loci that encode proteins of the cartilage extracellular matrix David L. RimoinI. Merete RasmussenDaniel H. Cohn Original Investigations Pages: 236 - 242
The utilization of interphase cytogenetic analysis for the detection of mosaicism Brenda L. LomaxDagmar K. KalousekHolly Safavi Original Investigations Pages: 243 - 247
Isolation and mapping of cosmid markers on human chromosome 22, including one within the submicroscopically deleted region of DiGeorge syndrome Hiroki KurahashiKenzo AkagiIsamu Nishisho Original Investigations Pages: 248 - 254
Molecular analysis of esterase D polymorphism Shuichi TsuchidaEmiko FukuiShigenori Ikemoto Original Investigations Pages: 255 - 258
Four novel mutant alleles of the arylsulfatase B gene in two patients with intermediate form of mucopolysaccharidosis VI (Maroteaux-Lamy syndrome) Elena VoskoboevaDirk IsbrandtChristoph Peters Original Investigations Pages: 259 - 264
Contiguous deletion and duplication mutations resulting in type 1 hereditary angioneurotic edema John J. BisslerVirginia H. DonaldsonAlvin E. Davis III Original Investigations Pages: 265 - 269
Isolation of two isoforms of the PAX3 gene transcripts and their tissue-specific alternative expression in human adult tissues Kazuhiro TsukamotoYusuke NakamuraNorio Niikawa Original Investigations Pages: 270 - 274
The spatial localization of homologous chromosomes in human fibroblasts at mitosis Andrew R. LeitchJames K. M. BrownJ. S. Heslop-Harrison Original Investigations Pages: 275 - 280
Mutation in a splice-donor site of the APC gene in a family with polyposis and late age of colonic cancer death L. VarescoV. GismondiG. B. Ferrara Original Investigations Pages: 281 - 286
Mutation screening by a combination of biotin-SSCP and direct sequencing Amarjit S. VirdiJohn A. LoughlinBryan C. Sykes Original Investigations Pages: 287 - 290
Refining the genetic map for the region flanking the X-linked hypophosphataemic rickets locus (Xp22.1–22.2) P. S. N. RoweJ. GouldingJ. L. H. O'Riordan Original Investigations Pages: 291 - 294
Chromosomal damage in sperm of patients surviving Hodgkin's disease following MOPP (nitrogen mustard, vincristine, procarbazine, and prednisone) therapy with and without radiotherapy B. F. BrandriffM. L. MeistrichJ. C. Liang Original Investigations Pages: 295 - 299
A 13 base pair deletion in exon 1 of HPRTIllinois forms a functional GUG initiation codon Beverly L. DavidsonNimrod GolovoyBlake J. Roessler Original Investigations Pages: 300 - 304
Linkage mapping of the spinal muscular atrophy gene Arthur H. M. BurghesSusan E. IngrahamJerry R. Mendell Original Investigations Pages: 305 - 312
A multiple interval physical map of the pericentromeric region of human chromosome 10 A. TunnacliffeM. S. JacksonB. A. J. Ponder Original Investigations Pages: 313 - 318
Human familial and sporadic breast cancer: analysis of the coding regions of the 17β-hydroxysteroid dehydrogenase 2 gene (EDH17B2) using a single-strand conformation polymorphism assay Arto MannermaaHellevi PeltoketoReijo Vihko Original Investigations Pages: 319 - 324
Prevalence of beta allele of the insulin gene in type II diabetes mellitus Wanda Horst-SikorskaBarbara ZollRyszard Slomski Original Investigations Pages: 325 - 328
Frequent polymorphism in exon 15 of the adenomatous polyposis coli gene Stella M. DaviesDale C. Snover Original Investigations Pages: 329 - 330
Coamplification on chromosomes 7p12-13 and 9q12-13 identified by reverse chromosome painting in a glioblastoma multiforme Ulrike FischerBernd WullichEckart Meese Original Investigations Pages: 331 - 334
Machado Joseph disease is not an allele of the spinocerebellar ataxia 2 locus Elspeth C. TwistLindsay A. FarrerGuy A. Rouleau Original Investigations Pages: 335 - 338
Homozygosity for a mutation in the lipoprotein lipase gene (Gly139→Ser) causes chylomicronaemia in a boy of Spanish descent Saskia M. BijvoetTaco BruinJohn J. P. Kastelein Original Investigations Pages: 339 - 343
Chronic childhood spinal muscular atrophy in Germany (West-Thüringen) — an epidemiological study Andrea ThiemeBeate MitullaAribert W. J. Spiegler Original Investigations Pages: 344 - 346
Nuclear-encoded subunits of human cytochrome c oxidase: SstI restriction fragment length polymorphism Suzanne A. AdjoaClaude BouchardFrance T. Dionne Short Communication Pages: 347 - 348
A new highly polymorphic DNA restriction site marker in the 5′ region of the human tyrosine hydroxylase gene (TH) detecting loss of heterozygosity in human embryonal rhabdomyosarcoma Corinne Besnard-GuérinWebster K. CaveneeIrene Newsham OriginalPaper Pages: 349 - 350
Two CA/GT repeat polymorphisms in intron 27 of the human neurofibromatosis type 1 (NF1) gene Conxi LázaroAntonia GaonaXavier Estivill OriginalPaper Pages: 351 - 352
An additional HpaII polymorphism in exon 2 of the human platelet membrane glycoprotein IIIa gene Bruno PerichonSylvie ClemenceauRajagopal Krishnamoorthy OriginalPaper Pages: 353 - 354
Insertion/deletion polymorphism within a polyadenylate stretch at the human atrial natriuretic peptides (hANP) gene locus Rajendranath RamasawmyChang Yong LuRajagopal Krishnamoorthy OriginalPaper Pages: 355 - 356
“Cryptic” dinucleotide polymorphism in the 3′ region of the factor IX gene shows substantial variation among different populations Steve S. SommerVictoria L. TillotsonCharyl M. Dutton OriginalPaper Pages: 357 - 358
Three CA/GT repeat polymorphisms from loci D21S414 and D21S1234 on human chromosome 21 Assumpció BoschStefan WiemannXavier Estivill OriginalPaper Pages: 359 - 360
Duplication of 1F and 1A2 genes in the vitamin D-binding protein (GC) system Toshihiro YasudaKoichiro Kishi Letters to the Editors Pages: 361 - 362
