Localization of the gene (or genes) for a syndrome with X-linked mental retardation, ataxia, weakness, hearing impairment, loss of vision and a fatal course in early childhood H. KremerB. C. J. HamelE. C. M. Mariman Original investigation Pages: 513 - 517
Dombrock blood group (DO): assignment to chromosome 12p H. EibergJan Mohr Original investigation Pages: 518 - 521
Sequence variations in the Fanconi anaemia gene, FAC: pathogenicity of 1806insA and R548X and recognition of D195V as a polymorphic variant Jerome R. Lo Ten FoeMartine T. BarelH. Joenje Original investigation Pages: 522 - 523
Deletion analysis of the SMN and NAIP genes in Kuwaiti patients with spinal muscular atrophy E. SamilchukBrendan D’SouzaSadika Al-Awadi Original investigation Pages: 524 - 527
Multiple products in the protein truncation test due to alternative splicing in the adenomatous polyposis coli (APC) gene Shashi BalaCornelia KrausW. G. Ballhausen Original investigation Pages: 528 - 533
Identification of NF2 germ-line mutations and comparison with neurofibromatosis 2 phenotypes L. KluweSaskia BayerV.-F. Mautner Original investigation Pages: 534 - 538
Absence of somatic mosaicism in 17 families with hemophilia B: an analysis with a sensitivity 10- to 1000-fold greater than that of sequencing gels Antje KnöllRhett P. KetterlingS. S. Sommer Original investigation Pages: 539 - 545
The apolipoprotein E polymorphism in Greenland Inuit in its global perspective L. U. GerdesChristian GerdesJørn Dyerberg Original investigation Pages: 546 - 550
HindIII DNA polymorphism in the lipoprotein lipase gene and plasma lipid phenotypes and carotid artery atherosclerosis Ling ChenWolfgang PatschE. Boerwinkle Original investigation Pages: 551 - 556
Hypertriglyceridemia and the apolipoprotein CIII gene locus: lack of association with the variant insulin response element in Italian school children C. C. ShouldersTamsin T. GranthamNancy J. Cox Original investigation Pages: 557 - 566
Age-dependent penetrance and mapping of the locus for juvenile and early-onset open-angle glaucoma on chromosome 1q (GLC1A) in a French family Anne MeyerAlain BéchetoilleH.-J. Garchon Original investigation Pages: 567 - 571
Exclusion of the MSX1 homeobox gene as the gene for the Ellis van Creveld syndrome in the Amish Susan E. IdeRosa Isela Ortiz De LunaR. I. Ortiz De Luna Original investigation Pages: 572 - 575
Molecular cytogenetic characterization of breakpoints involving pericentric inversions of human chromosome 9 R. V. SamonteRobert A. ConteR. S. Verma Original investigation Pages: 576 - 580
Molecular genetics of familial hypercholesterolemia in Israel Ayeleth ReshefHenrik NissenE. Leitersdorf Original investigation Pages: 581 - 586
Two novel mutations in the aquaporin-2 and the vasopressin V2 receptor genes in patients with congenital nephrogenic diabetes insipidus Alexander OkscheAndreas MöllerW. Rosenthal Original investigation Pages: 587 - 589
OB gene not linked to human obesity in Mexican American affected sib pairs from Starr County, Texas Molly S. BrayEric BoerwinkleC. L. Hanis Original investigation Pages: 590 - 595
The origin of the most common mutation of adenine phosphoribosyltransferase among Japanese goes back to a prehistoric era N. KamataniChihiro TeraiSadao Kashiwazaki Original investigation Pages: 596 - 600
Microsatellite instability and mutations of p53 and TGF-‚ RII genes in gastric cancer B. RenaultDaniele CalistriGuglielmina N. Ranzani Original investigation Pages: 601 - 607
Simultaneous detection of structural and numerical chromosome abnormalities in sperm of healthy men by multicolor fluorescence in situ hybridization P. Van HummelenX. R. LoweAndrew J. Wyrobek Original investigation Pages: 608 - 615
Sequence-specific and length-dependent interaction of C2H2 zinc fingers and (TA)n microsatellites Joseph A. GogosMaria Karayiorgou Rapid communication Pages: 616 - 619
Linkage disequilibrium analysis in Machado-Joseph disease patients of different ethnic origins Claudia GasparIscia Lopes-CendesG. A. Rouleau Rapid communication Pages: 620 - 624
Twelve amplified and expressed genes localized in a single domain in glioma Ulrike FischerPaul MeltzerE. Meese Rapid communication Pages: 625 - 628
