1. Viral integration, fragile sites, and proto-oncogenes in human neoplasia

   • Nicholas C. Popescu
   • Drazen Zimonjic
   • Joseph A. DiPaolo

   Original Investigations Pages: 383 - 386

2. Recurrent nonsense mutations at arginine residues cause severe hemophilia B in unrelated hemophiliacs

   • D. D. Koeberl
   • C. D. K. Bottema
   • S. S. Sommer

   Original Investigations Pages: 387 - 390

3. Localization of the human HF.10 finger gene on a chromosome region (3p21–22) frequently deleted in human cancers

   • Emilio Donti
   • Luisa Lanfrancone
   • Pier Giuseppe Pelicci

   Original Investigations Pages: 391 - 395

4. 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. Kastelein
   • Jonathan L. Haines
   • Michael R. Hayden

   Original Investigations Pages: 396 - 400

5. Investigation of factor VIII:C gene restriction fragment length polymorphisms and search for deletions in hemophiliac subjects in Algeria

   • K. Nafa
   • F. Meriane
   • M. Delpech

   Original Investigations Pages: 401 - 405

6. 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-Hansen
   • L. L. Field
   • W. G. Pearce

   Original Investigations Pages: 406 - 408

7. Phenylketonuria mutation in Chinese haplotype 44 identical with haplotype 2 mutation in northern-European Caucasians

   • Ting-Fen Tsai
   • Kwang-Jen Hsiao
   • Tsung-Sheng Su

   Original Investigations Pages: 409 - 411

8. Use of three DNA polymorphisms of the LDL receptor gene in the diagnosis of familial hypercholesterolemia

   • A. Daga
   • T. Mattioni
   • S. Bertolini

   Original Investigations Pages: 412 - 416

9. Isolation and regional localisation of DNA sequences from a human chromosome 11-specific cosmid library

   • Roy B. Wadey
   • Peter F. R. Little
   • John K. Cowell

   Original Investigations Pages: 417 - 423

10. Telomere association of chromosomes induced by aphidicolin in a normal individual

    • C. Fuster
    • R. Miró
    • J. Egozcue

    Original Investigations Pages: 424 - 426

11. Chromosomal in situ hybridization of a Hodgkin's disease-derived cell line (L540) using DNA probes for TCRA, TCRB, MET, and rRNA

    • Christa Fonatsch
    • Georg Gradl
    • Hans Tesch

    Original Investigations Pages: 427 - 434

12. Genetic differences in cystic fibrosis patients with and without pancreatic insufficiency

    • Maurizio Ferrari
    • Mariano Antonelli
    • Robert Williamson

    Original Investigations Pages: 435 - 438

13. Apolipoprotein A1 Baltimore (Arg₁₀→Leu), a new ApoA1 variant

    • John A. A. Ladias
    • Peter O. Kwiterovich Jr.
    • Stylianos E. Antonarakis

    Original Investigations Pages: 439 - 445

14. In situ hybridization studies using a molecular probe that maps to Xq27–Xq28

    • Alessandra M. V. Duncan
    • Clive Morgan

    Original Investigations Pages: 446 - 448

15. Studies of RFLP closely linked to the cystic fibrosis locus throughout Europe lead to new considerations in populations genetics

    • J. L. Serre
    • B. Simon-Bouy
    • A. Boué

    Original Investigations Pages: 449 - 454

16. Trophoblast glycoprotein recognised by monoclonal antibody 5T4 maps to human chromosome 6q14–q15

    • J. M. Boyle
    • K. H. Grzeschik
    • P. L. Stern

    Original Investigations Pages: 455 - 458

17. Choroideremia associated with an X-autosomal translocation

    • Victoria M. Siu
    • John R. Gonder
    • Wayne F. Flintoff

    Original Investigations Pages: 459 - 464

18. Isolation of a cDNA clone encoding a novel form of granzyme B from human NK cells and mapping to chromosome 14

    • Carol A. Dahl
    • Fritz H. Bach
    • J. Scott Cairns

    Original Investigations Pages: 465 - 470

19. A PvuII restriction fragment length polymorphism of the glucose-6-phosphate dehydrogenase gene is an African-specific marker

    • Martin F. Fey
    • Jim S. Wainscoat
    • Lucio Luzzatto

    Short Communications Pages: 471 - 472

20. The human homeobox gene HOX7 maps to chromosome 4p16.1 and may be implicated in Wolf-Hirschhorn syndrome

    • Alasdair Ivens
    • Nora Flavin
    • Benoit Robert

    Short Communications Pages: 473 - 476

21. Regional assignment of the human C1-inhibitor gene to 11q11–q13.1

    • A. Theriault
    • K. Whaley
    • J. M. Connor

    Short Communications Pages: 477 - 479

22. A common Chinese β-thalassemia mutation found in a Japanese family

    • Yuji Naritomi
    • Hitoshi Nakashima
    • Takashi Imamura

    Short Communications Pages: 480 - 482

23. Hypoxanthine guanine phosphoribosyltransferase deficiency: nucleotide substitution causing Lesch-Nyhan syndrome identified for the first time among Japanese

    • Shin Fujimori
    • Naoyuki Kamatani
    • Ieo Akaoka

    Short Communications Pages: 483 - 486

24. Germinal mosaicism in Crouzon syndrome

    • Sven Kreiborg
    • M. Michael Cohen Jr.

    Clinical Case Report Pages: 487 - 488

25. An NcoI restriction fragment length polymorphism at the human steroid sulphatase gene locus

    • Peter M. van Zandvoort
    • Cor A. van Bennekom
    • Bernard A. van Oost

    DNA Variants Pages: 489 - 490

26. The “polyclonal hyperimmunoglobulin G1(A1) syndrome” is a secondary phenomenon due to autoimmune disease

    • M. J. Krol-van Straaten
    • H. C. M. Haanen
    • C. E. M. de Maat

    Letters to the Editors Pages: 491 - 492