An apolipoprotein CIII marker associated with hypertriglyceridemia in Caucasians also confers increased risk in a west Japanese population Qing ZengMarilyn DammermanJun Sasaki Original Investigation Pages: 371 - 375
Mucopolysaccharidosis IVA: structural gene alterations identified by Southern blot analysis and identification of racial differences Shunji TomatsuSeiji FukudaTadao Orii Original Investigation Pages: 376 - 381
Exclusion of the cone-specific α-subunit of the transducin gene in Stargardt's disease Sylvie GerberJean-Michel RozetJosseline Kaplan Original Investigation Pages: 382 - 384
Heterogeneity of the apolipoprotein H *3 allele and its role in affecting the binding of apolipoprotein H (β2-glycoprotein I) to anionic phospholipids M. Ilyas KambohDawn R. WagenknechtJohn A. McIntyre Original Investigation Pages: 385 - 388
Polymorphisms in the human DNA polymerase β gene Yasushi DobashiYoshinobu KubotaMasahiko Hosaka Original Investigation Pages: 389 - 390
Human ferrochelatase: a novel mutation in patients with erythropoietic protoporphyria and an isoform caused by alternative splicing Xiaoye Schneider-YinBeat W. SchäferElisabeth I. Minder Original Investigation Pages: 391 - 396
Analysis of the complete coding region of the CFTR gene in a cohort of CF patients from North-Eastern Italy: identification of 90% of the mutations Alberto BonizzatoElena NicolisPier Franco Pignatti Original Investigation Pages: 397 - 402
Detection of a germline mutation at codon 918 of the RET proto-oncogene in French MEN 2B families Mireille RosselColette BonnardelGiovanni Romeo Original Investigation Pages: 403 - 406
Molecular basis and PCR-DNA typing of the Fya/fyb blood group polymorphism Christophe TournamilleCaroline Le Van KimYves Colin Original Investigation Pages: 407 - 410
Benign familial neonatal convulsions: confirmation of genetic heterogeneity and further evidence for a second locus on chromosome 8q Ortrud SteinleinVolker SchusterMartin Häussier Original Investigation Pages: 411 - 415
Genetic heterogeneity in adult dominant polycystic kidney disease in Cypriot families C. D. Constantinou-DeltasElena PapageorgiouAlkis Pierides Original Investigation Pages: 416 - 423
A new mutation of the ALAS2 gene in a large family with X-linked sideroblastic anemia Emmanuel PradesCécile ChambonBernard Grandchamp Original Investigation Pages: 424 - 428
New polymorphisms and markers in the HLA class I region: relevance to hereditary hemochromatosis (HFE) Angela TotaroAnna GrifaPaolo Gasparini Original Investigation Pages: 429 - 434
Molecular basis of inter-alpha-trypsin inhibitor heavy chain H1 (ITIH1) polymorphism M. DingK. UmetsuT. Suzuki Short Communication Pages: 435 - 436
Non-radioactive multiplex-SSCP analysis: detection of a new type II procollagen gene (COL2A1) mutation Andreas WinterpachtKatja HilbertBernhard Zabel Short Communication Pages: 437 - 439
Molecular characterisation of the glucose-6-phosphate dehydrogenase (G6PD) Ferrara II variant Maria Domenica CappelliniFranco Martinez di MontemurosGemino Fiorelli Short Communication Pages: 440 - 442
A 163-bp deletion at the C-terminus of the schwannomin gene associated with variable phenotypes of neurofibromatosis type 2 Lan KluweStefan M. PulstVictor -F. Mautner Short Communication Pages: 443 - 446
A novel missense mutation (Thr176→IIe) at the putative hinge of the neo N-terminus of activated protein C Paula J. HallamAdam I. WaceyDavid N. Cooper Short Communication Pages: 447 - 450
A high-density microsatellite map of the ataxia-telangiectasia locus Lina VanagaiteMichael R. JamesYosef Shiloh Short Communication Pages: 451 - 454
Exclusion of the 13-kDa rapamycin binding protein gene (FKBP2) as a candidate gene for multiple endocrine neoplasia type 1 Sean GrimmondGunther WeberNick Hayward Short Communication Pages: 455 - 458
Identification of a PstI polymorphism in the p21Cip1/Waf1 cyclin-dependent kinase inhibitor gene John C. LawAnee Deka DNA Variants Pages: 459 - 460
Mval polymorphism in the proteolipid protein (PLP) gene Hitoshi OsakaKen InoueKenji Kosaka DNA Variants Pages: 461 - 461
Fluorescent multiplex microsatellites used to identify haplotype associations with 15 CFTR mutations in 124 Northern Irish CF families David HughesAlison HillColin Graham DNA Variants Pages: 462 - 464
A new polymorphism in exon 7 of the cystic fibrosis transmembrane regulator (CFTR) gene Lidija PetreskaSvetlana KočevaGeorgi Dimitar Efremov DNA Variants Pages: 465 - 466
Dinucleotide polymorphism at the DXS1178 locus is tightly linked to PGK1 at Xq13 Ricardo FujitaCraig SkolnickAnand Swaroop DNA Variants Pages: 467 - 468
Dinucleotide repeat polymorphism within the PHKA1 gene at Xq12-q13 Martin GossenAndrea WüllrichManfred W. Kilimann DNA Variants Pages: 469 - 470
Polymorphism of the pentanucleotide repeat d(AAAAT) within intron 1 of the human tumor suppressor gene p53 (17p13.1) Meinhard HahnRainer FislageAlfred Pingoud DNA Variants Pages: 471 - 472
C to T and/or G to A transitions are responsible for loss of a MspI restriction site at the 5′-end of the human apolipoprotein AI gene X. L. WangR. BadenhopD. E. L. Wilcken DNA Variants Pages: 473 - 474
Two polymorphic dinucleotide repeats in intron 44 of the dystrophin gene Silvia KöchlingJohan T. den DunnenJürgen Horst DNA Variants Pages: 475 - 477