1. Isolated supravalvular aortic stenosis: functional haploinsufficiency of the elastin gene as a result of nonsense-mediated decay

   • Zsolt Urbán
   • Virginia V. Michels
   • Charles D. Boyd

   Original Investigation 18 May 2000 Pages: 577 - 588

2. The ALDH2 genotype, alcohol intake, and liver-function biomarkers among Japanese male workers

   • Tatsuya Takeshita
   • Xing Yang
   • Kanehisa Morimoto

   Original investigation 01 June 2000 Pages: 589 - 593

3. Exclusion of NFIL3 as the gene causing hereditary sensory neuropathy type I by mutation analysis

   • Dennis J. Hulme
   • Ian P. Blair
   • Garth A. Nicholson

   Original Investigation 13 May 2000 Pages: 594 - 596

4. Analysis of CAG repeats in SCA1, SCA2, SCA3, SCA6, SCA7 and DRPLA loci in spinocerebellar ataxia patients and distribution of CAG repeats at the SCA1, SCA2 and SCA6 loci in nine ethnic populations of eastern India

   • Priyadarshi Basu
   • Biswanath Chattopadhyay
   • Nitai P. Bhattacharyya

   Original Investigation 01 June 2000 Pages: 597 - 604

5. Two pregnancies after preimplantation genetic diagnosis for osteogenesis imperfecta type I and type IV

   • Anick De Vos
   • Karen Sermon
   • André Van Steirteghem

   Original Investigation 01 June 2000 Pages: 605 - 613

6. Genomic organisation and chromosomal localisation of two members of the KCND ion channel family, KCND2 and KCND3

   • Alex V. Postma
   • Connie R. Bezzina
   • Marcel M. A. M. Mannens

   Original Investigation 19 May 2000 Pages: 614 - 619

7. Mechanisms of maternal aneuploidy: FISH analysis of oocytes and polar bodies in patients undergoing assisted conception

   • Radma Mahmood
   • Catherine H. Brierley
   • Joy D. A. Delhanty

   Original Investigation 26 May 2000 Pages: 620 - 626

8. Gene structures of the human non-neuronal monoamine transporters EMT and OCT2

   • Dirk Gründemann
   • Edgar Schömig

   Original Investigation 19 May 2000 Pages: 627 - 635

9. Confirmation of linkage of Duane's syndrome and refinement of the disease locus to an 8.8-cM interval on chromosome 2q31

   • Julie Claire Evans
   • Timothy Mark Frayling
   • Nick J. Gutowski

   Original Investigation 19 May 2000 Pages: 636 - 638

10. Structure and polymorphism of the human gene for the interferon-induced p78 protein (MX1): evidence of association with alopecia areata in the Down syndrome region

    • Rachid Tazi-Ahnini
    • Francesco S. di Giovine
    • Michael J. Cork

    Original Investigation 31 May 2000 Pages: 639 - 645

11. Molecular genetic analysis of severe protein C deficiency

    • David S. Millar
    • Bent Johansen
    • David N. Cooper

    Original Investigation 31 May 2000 Pages: 646 - 653

12. Mutations in the 4-hydroxyphenylpyruvate dioxygenase gene (HPD) in patients with tyrosinemia type III

    • Ulla Rüetschi
    • Roberto Cerone
    • Elisabeth Holme

    Original Investigation 25 May 2000 Pages: 654 - 662

13. Application and evaluation of denaturing HPLC for molecular genetic analysis in tuberous sclerosis

    • Alistair C. Jones
    • Julian R. Sampson
    • Jeremy P. Cheadle

    Original Investigation 30 May 2000 Pages: 663 - 668

14. Acquired pericentric inversion of chromosome 9 in essential thrombocythemia

    • T. S. K. Wan
    • S. K. Ma
    • L. C. Chan

    Letter to the Editor 19 May 2000 Pages: 669 - 670