Localisation of the classical DNA satellites on human chromosomes as determined by primed in situ labelling (PRINS) A. J. TherkelsenA. NielsenS. Kølvraa Original investigation Pages: 322 - 326
Interaction between obesity and genetic polymorphisms in the apolipoprotein CIII gene and lipoprotein lipase gene on the risk of hypertriglyceridemia in Chinese Y.-L. KoYu-Shien KoYing-Shiung Lee Original investigation Pages: 327 - 333
A de novo complex t(7;13;8) translocation with a deletion in the TRPS gene region C. A. BrandtHermann-Josef LüdeckeUrsula Friedrich Original investigation Pages: 334 - 338
CAG repeat analyses in frozen and formalin-fixed tissues following primer extension preamplification for evaluation of mitotic instability of expanded SCA1 alleles C. ZühlkeYorck HellenbroichEberhard Schwinger Original investigation Pages: 339 - 344
Loss of the PLA2G2A gene in a sporadic colorectal tumor of a patient with a PLA2G2A germline mutation and absence of PLA2G2A germline alterations in patients with FAP Inko NimmrichWaltraut FriedlO. Müller Original investigation Pages: 345 - 349
The STR252 – IVS10nt546 – VNTR7 phenylalanine hydroxylase minihaplotype in five Mediterranean samples Francesco CalìIrma DianzaniV. Romano Original investigation Pages: 350 - 355
The long QT syndrome: a novel missense mutation in the S6 region of the KVLQT1 gene M. H. van den BergArthur A. M WildeJoep P. M. Geraedts Original investigation Pages: 356 - 361
Hereditary nonpolyposis colorectal cancer: causative role of a germline missense mutation in the hMLH1 gene confirmed by the independent occurrence of the same somatic mutation in tumour tissue Y. WangW. FriedlPeter Propping Original investigation Pages: 362 - 364
Distinct spectrum of CFTR gene mutations in congenital absence of vas deferens T. DörkBernd DworniczakManfred Stuhrmann Original investigation Pages: 365 - 377
Progressive familial intrahepatic cholestasis (PFIC): evidence for genetic heterogeneity by exclusion of linkage to chromosome 18q21–q22 Henrik ArnellAntal NemethN. Dahl Original investigation Pages: 378 - 381
Benign recurrent intrahepatic cholestasis (BRIC): evidence of genetic heterogeneity and delimitation of the BRIC locus to a 7-cM interval between D18S69 and D18S64 Richard J. SinkeVictoria E. H. CarltonRoderick H. J. Houwen Original investigation Pages: 382 - 387
Supernumerary nipples occurring together with Becker’s naevus: an association involving one common paradominant trait? Carlo Enrico UrbaniRoberto Betti Original investigation Pages: 388 - 390
Screening for connexin 32 mutations in Charcot-Marie-Tooth disease families with possible X-linked inheritance K. SilanderPäivi MeretojaMarja-Liisa Savontaus Original investigation Pages: 391 - 397
Localization of a novel human RNA-editing deaminase (hRED2 or ADARB2) to chromosome 10p15 Lauréane MittazStylianos E. AntonarakisH. S. Scott Original investigation Pages: 398 - 400
Detection of chromosomal aneuploidy in endometriosis by multi-color fluorescence in situ hybridization (FISH) Jong-Chul ShinHelen L. RossF. Z. Bischoff Original investigation Pages: 401 - 406
Trinucleotide repeats (CGG)22TGG(CGG)43TGG(CGG)21 from the fragile X gene remain stable in transgenic mice Christian N. LavedanLisa GarrettR. L. Nussbaum Original investigation Pages: 407 - 414
Molecular studies in 37 Silver-Russell syndrome patients: frequency and etiology of uniparental disomy T. EggermannHartmut A. WollmannMichael B. Ranke Original investigation Pages: 415 - 419
Angiotensin-converting enzyme (ACE) gene polymorphisms in patients characterised by coronary angiography Carole A. FoyGillian I. RiceP. J. Grant Original investigation Pages: 420 - 425
Localization of the gene for Wieacker-Wolff syndrome in the pericentromeric region of the X chromosome D.-U. KloosS. JakubiczkaP. Wieacker Original investigation Pages: 426 - 430
Chromosomal instability in a woman with infertility and two unaffected brothers: a new familial chromosomal breakage syndrome? H.-C. DubaHarald G. WeirichGerd Utermann Original investigation Pages: 431 - 440
Molecular cloning of the breakpoints of the hereditary persistence of fetal hemoglobin type-6 (HPFH-6) deletion and sequence analysis of the novel juxtaposed region from the 3′ end of the β-globin gene cluster Theodoros KosteasAntonella PalenaN. P. Anagnou Original investigation Pages: 441 - 445
Quantification of the paternal allele bias for new germline mutations in the retinoblastoma gene T. P. DryjaJennifer F. MorrowJoyce M. Rapaport Original investigation Pages: 446 - 449
Adult onset globoid cell leukodystrophy (Krabbe disease): analysis of galactosylceramidase cDNA from four Japanese patients H. FuruyaYoh-ji KukitaTakuro Kobayashi Original investigation Pages: 450 - 456
Human transferrin (Tf): a single mutation at codon 570 determines Tf C1 or Tf C2 variant Kazuhiko NamekataFumitaka OyamaY. Ihara Original investigation Pages: 457 - 458
Evidence that skewed X inactivation is not needed for the phenotypic expression of Aicardi syndrome H. M. HoagS. A. M. TaylorM. M. Khalifa Original investigation Pages: 459 - 464
α-Thalassemia in The Netherlands: a heterogeneous spectrum of both deletions and point mutations K. L. HarteveldMonique LosekootLuigi F. Bernini Original investigation Pages: 465 - 471
Removal of repetitive sequences from FISH probes using PCR-assisted affinity chromatography J. M. CraigJürgen KrausThomas Cremer Rapid communication Pages: 472 - 476
Mapping of a novel SH3 domain protein and two proteins of unknown function to human chromosome 21 Nicholas KatsanisJonathan A. BeckE. M. C. Fisher Rapid communication Pages: 477 - 480
Mapping of the gene encoding the B56β subunit of protein phosphatase 2A (PPP2R5B) to a 0.5-Mb region of chromosome 11q13 and its exclusion as a candidate gene for multiple endocrine neoplasia type 1 (MEN1) The European Consortium on MEN1S. A. ForbesK. Kas Rapid communication Pages: 481 - 485
The plakophilin 1 (PKP1) and plakoglobin (JUP) genes map to human chromosomes 1q and 17, respectively Catherine M. E. CowleyDanijela SimrakR. S. Buxton Letter to the editors Pages: 486 - 488