Molecular biology of hypophosphataemic rickets and oncogenic osteomalacia Peter. S. N. Rowe Review Article Pages: 457 - 467
Multiple endocrine neoplasia type 1 (MEN1) in two Asian families B. T. TehS. I. HiiN. K. Hayward Original Investigation Pages: 468 - 472
Large DNA inversions, deletions, and TaqI site mutations in severe haemophilia A Mauro S. FigueiredoMarti H. TavellaBelinda P. Simões Original Investigation Pages: 473 - 478
The fragile X syndrome in Finland: demonstration of a founder effect by analysis of microsatellite haplotypes Rutva HaatajaMarja-Leena VäisänenJaakko Leisti Original Investigation Pages: 479 - 483
Putative non-Mendelian transmission of retinoblastoma in males: a phenotypic segregation analysis of 150 pedigrees F. L. MunierA. L. MurphreeH. P. Rutz Original Investigation Pages: 484 - 490
Frequency and parental origin of hypermethylated RB1 alleles in retinoblastoma Valerie GregerNils DebusBernhard Horsthemke Original Investigation Pages: 491 - 496
Three unrelated individuals with perinatally lethal osteogenesis imperfecta resulting from identical Gly502Ser substitutions in the α2-chain of type I collagen Nicola J. RoseKatrina MackayRaymond Dalgleish Original Investigation Pages: 497 - 503
Fluorescence in situ hybridization reveals a break in the α-satellite DNA of chromosome 1 in a family with a balanced whole-arm translocation C. H. GravholtM. CapraniU. Friedrich Original Investigation Pages: 504 - 508
Three novel missense mutations in the antithrombin III (AT3) gene causing recurrent venous thrombosis David S. MillarAdam I. WaceyDavid N. Cooper Original Investigation Pages: 509 - 512
At least five polymorphic mutants account for the prevalence of glucose-6-phosphate dehydrogenase deficiency in Algeria Khedoudja NafaAbderrezak ReghisLucio Luzzatto Original Investigation Pages: 513 - 517
Fluorescence in situ hybridization on paraffin-embedded abortion material as a means of retrospective chromosome analysis Gesina van LijnschotenJozefa AlbrechtsJoseph P. M. Geraedts Original Investigation Pages: 518 - 522
Apparent regression of the CGG repeat in FMR1 to an allele of normal size Lieve VitsKristel De BoullePatrick J. Willems Original Investigation Pages: 523 - 526
Mammalian adenylyl cyclase family members are randomly located on different chromosomes Christophe GaudinCharles J. HomeyYoshihiro Ishikawa Original Investigation Pages: 527 - 529
Filipino β-thalassemia due to a large deletion: identification of the deletion end points and polymerase chain reaction (PCR)-based diagnosis John S. WayeBarry EngDavid H. K. Chui Original Investigation Pages: 530 - 532
Detection of more than 50 different CFTR mutations in a large group of German cystic fibrosis patients Thilo DörkFrauke MekusBurkhard Tümmler Original Investigation Pages: 533 - 542
Genotype-phenotype correlation between position of constitutional APC gene mutation and CHRPE expression in familial adenomatous polyposis Yvonne L. WallisFiona MacdonaldDion G. Morton Original Investigation Pages: 543 - 548
Mapping of the human C3G gene coding a guanine nucleotide releasing protein for Ras family to 9q34.3 by fluorescence in situ hybridization Setsuo TakaiMasamitsu TanakaMichiyuki Matsuda Short Communication Pages: 549 - 550
Genetic heterogeneity in hypokalemic periodic paralysis (hypoPP) Emmanuelle PlassartAlexis ElbazBertrand Fontaine Short Communication Pages: 551 - 556
Localization of the human coproporphyrinogen oxidase gene to chromosome band 3q12 Valère CacheuxPavel MartasekBernard Grandchamp Short Communication Pages: 557 - 559
A novel single-base mutation in the glucose 6-phosphate dehydrogenase gene is associated with chronic non-spherocytic haemolytic anaemia Stefonia FilosaWangwie CaiGiuseppe Martini Short Communication Pages: 560 - 562
Trinucleotide (CAG) repeat expansion in chromosomes of Spanish patients with Huntington's disease J. BenitezE. FernandezJ. Yebenes Short Communication Pages: 563 - 564
Genetic and physical mapping of the GLUR5 glutamate receptor gene on human chromosome 21 Paul GregorSandra M. GastonRobert H. Brown Jr. Short Communication Pages: 565 - 570
Gene frequencies of alcohol dehydrogenase2 (ADH2) and aldehyde dehydrogenase2 (ALDH2) in five Chinese minorities Shi-Han ChenMin ZhangC. Ronald Scott Short Communication Pages: 571 - 572
Preliminary mutation analysis in the phenylanaline hydroxylase gene in Greek PKU and HPA patients J. Traeger-SynodinosE. KanavakisC. Kattamis Short Communication Pages: 573 - 575
The gene causing familial mediterranean fever maps to the short arm of chromosome 16 in Druze and Moslem Arab families Elon PrasIvona AksentijevichDaniel L. Kastner Short Communication Pages: 576 - 577
A new complex polymorphic repeat close to the HLA-A and HLA-E loci Angela TotaroAnna GrifaPaolo Gasparini OriginalPaper Pages: 578 - 578
A novel polymorphism in the coding sequence of the human RET proto-oncogene Patrick EderyTania AttiéStanislas Lyonnet OriginalPaper Pages: 579 - 580
A unique mutation underlying carbonic anhydrase II deficiency syndrome in patients of Arab descent Dahmani M. FathallahMohamed BejaouiKoussay Dellagi OriginalPaper Pages: 581 - 582
An insertion/deletion polymorphism at the D15S63 locus in the critical Prader-Willi syndrome region in 15q11-13 Bärbel DittrichKarin BullingBernhard Horsthemke OriginalPaper Pages: 583 - 584
A pentanucleotide tandem duplication polymorphism in the 3′ untranslated region of the HLA-linked heat-shock protein 70-2 (HSP70-2) gene Ralf DresselEberhard Günther OriginalPaper Pages: 585 - 586
