Viral integration, fragile sites, and proto-oncogenes in human neoplasia Nicholas C. PopescuDrazen ZimonjicJoseph A. DiPaolo Original Investigations Pages: 383 - 386
Recurrent nonsense mutations at arginine residues cause severe hemophilia B in unrelated hemophiliacs D. D. KoeberlC. D. K. BottemaS. S. Sommer Original Investigations Pages: 387 - 390
Localization of the human HF.10 finger gene on a chromosome region (3p21–22) frequently deleted in human cancers Emilio DontiLuisa LanfranconePier Giuseppe Pelicci Original Investigations Pages: 391 - 395
The gene causing familial hypoalphalipoproteinemia is not caused by a defect in the apo AI-CIII-AIV gene cluster in a Spanish family John J. P. KasteleinJonathan L. HainesMichael R. Hayden Original Investigations Pages: 396 - 400
Investigation of factor VIII:C gene restriction fragment length polymorphisms and search for deletions in hemophiliac subjects in Algeria K. NafaF. MerianeM. Delpech Original Investigations Pages: 401 - 405
A locus for X-linked congenital stationary night blindness is located on the proximal portion of the short arm of the X chromosome N. T. Bech-HansenL. L. FieldW. G. Pearce Original Investigations Pages: 406 - 408
Phenylketonuria mutation in Chinese haplotype 44 identical with haplotype 2 mutation in northern-European Caucasians Ting-Fen TsaiKwang-Jen HsiaoTsung-Sheng Su Original Investigations Pages: 409 - 411
Use of three DNA polymorphisms of the LDL receptor gene in the diagnosis of familial hypercholesterolemia A. DagaT. MattioniS. Bertolini Original Investigations Pages: 412 - 416
Isolation and regional localisation of DNA sequences from a human chromosome 11-specific cosmid library Roy B. WadeyPeter F. R. LittleJohn K. Cowell Original Investigations Pages: 417 - 423
Telomere association of chromosomes induced by aphidicolin in a normal individual C. FusterR. MiróJ. Egozcue Original Investigations Pages: 424 - 426
Chromosomal in situ hybridization of a Hodgkin's disease-derived cell line (L540) using DNA probes for TCRA, TCRB, MET, and rRNA Christa FonatschGeorg GradlHans Tesch Original Investigations Pages: 427 - 434
Genetic differences in cystic fibrosis patients with and without pancreatic insufficiency Maurizio FerrariMariano AntonelliRobert Williamson Original Investigations Pages: 435 - 438
Apolipoprotein A1 Baltimore (Arg10→Leu), a new ApoA1 variant John A. A. LadiasPeter O. Kwiterovich Jr.Stylianos E. Antonarakis Original Investigations Pages: 439 - 445
In situ hybridization studies using a molecular probe that maps to Xq27–Xq28 Alessandra M. V. DuncanClive Morgan Original Investigations Pages: 446 - 448
Studies of RFLP closely linked to the cystic fibrosis locus throughout Europe lead to new considerations in populations genetics J. L. SerreB. Simon-BouyA. Boué Original Investigations Pages: 449 - 454
Trophoblast glycoprotein recognised by monoclonal antibody 5T4 maps to human chromosome 6q14–q15 J. M. BoyleK. H. GrzeschikP. L. Stern Original Investigations Pages: 455 - 458
Choroideremia associated with an X-autosomal translocation Victoria M. SiuJohn R. GonderWayne F. Flintoff Original Investigations Pages: 459 - 464
Isolation of a cDNA clone encoding a novel form of granzyme B from human NK cells and mapping to chromosome 14 Carol A. DahlFritz H. BachJ. Scott Cairns Original Investigations Pages: 465 - 470
A PvuII restriction fragment length polymorphism of the glucose-6-phosphate dehydrogenase gene is an African-specific marker Martin F. FeyJim S. WainscoatLucio Luzzatto Short Communications Pages: 471 - 472
The human homeobox gene HOX7 maps to chromosome 4p16.1 and may be implicated in Wolf-Hirschhorn syndrome Alasdair IvensNora FlavinBenoit Robert Short Communications Pages: 473 - 476
Regional assignment of the human C1-inhibitor gene to 11q11–q13.1 A. TheriaultK. WhaleyJ. M. Connor Short Communications Pages: 477 - 479
A common Chinese β-thalassemia mutation found in a Japanese family Yuji NaritomiHitoshi NakashimaTakashi Imamura Short Communications Pages: 480 - 482
Hypoxanthine guanine phosphoribosyltransferase deficiency: nucleotide substitution causing Lesch-Nyhan syndrome identified for the first time among Japanese Shin FujimoriNaoyuki KamataniIeo Akaoka Short Communications Pages: 483 - 486
Germinal mosaicism in Crouzon syndrome Sven KreiborgM. Michael Cohen Jr. Clinical Case Report Pages: 487 - 488
An NcoI restriction fragment length polymorphism at the human steroid sulphatase gene locus Peter M. van ZandvoortCor A. van BennekomBernard A. van Oost DNA Variants Pages: 489 - 490
The “polyclonal hyperimmunoglobulin G1(A1) syndrome” is a secondary phenomenon due to autoimmune disease M. J. Krol-van StraatenH. C. M. HaanenC. E. M. de Maat Letters to the Editors Pages: 491 - 492
