1. A genome-wide search for genes predisposing to familial psoriasis by using a stratification approach

   • L. Samuelsson
   • F. Enlund
   • T. Martinsson

   Original Investigation 04 November 1999 Pages: 523 - 529

2. BamHI-SacI RFLP and Gm analysis of the immunoglobulin IGHG genes in the Northern Selkups (west Siberia): new haplotypes with deletion, duplication and triplication

   • L.P. Osipova
   • O.L. Posukh
   • M.-P. Lefranc

   Original Investigation 17 November 1999 Pages: 530 - 541

3. Association between monoamine oxidase A activity in human male skin fibroblasts and genotype of the MAOA promoter-associated variable number tandem repeat

   • R.M. Denney
   • H. Koch
   • I.W. Craig

   Original Investigation 04 November 1999 Pages: 542 - 551

4. A novel gene containing LIM domains (LIMD1) is located within the common eliminated region 1 (C3CER1) in 3p21.3

   • H. Kiss
   • D. Kedra
   • J.P. Dumanski

   Original Investigation 17 November 1999 Pages: 552 - 559

5. Two novel mutations of SURF1 in Leigh syndrome with cytochrome c oxidase deficiency

   • M. Teraoka
   • Y. Yokoyama
   • Y. Seino

   Original Investigation 16 November 1999 Pages: 560 - 563

6. Correlation between human papillomavirus-associated cervical cancer and p53 codon 72 arginine/proline polymorphism

   • R. Tachezy
   • I. Mikyšková
   • M. Van Ranst

   Original Investigation 23 October 1999 Pages: 564 - 566

7. Minisatellite mutational processes reduce F_st estimates

   • J. Flint
   • J. Bond
   • R. M. Harding

   Original Investigation 05 November 1999 Pages: 567 - 576

8. High throughput analysis of 10 microsatellite and 11 diallelic polymorphisms on the human Y-chromosome

   • M.G. Thomas
   • N. Bradman
   • H.M. Flinn

   Original Investigation 04 November 1999 Pages: 577 - 581

9. Genomic characterization of the human peptidyl-prolyl-cis-trans-isomerase, mitochondrial precursor gene: assessment of its role in familial dilated cardiomyopathy

   • K.R. Bowles
   • C. Zintz
   • J.A. Towbin

   Original Investigation 26 October 1999 Pages: 582 - 586

10. Molecular analysis of eight mutations in FBN1

    • D. Halliday
    • S. Hutchinson
    • P. A. Handford

    Original Investigation 17 November 1999 Pages: 587 - 597

11. Screening for UBE3A gene mutations in a group of Angelman syndrome patients selected according to non-stringent clinical criteria

    • A. Baumer
    • D. Balmer
    • A. Schinzel

    Original Investigation 16 November 1999 Pages: 598 - 602

12. MEN I gene mutations in sporadic adrenal adenomas

    • K.-M. Schulte
    • M. Heinze
    • H.-D. Röher

    Original Investigation 16 November 1999 Pages: 603 - 610

13. Multiple small accessory marker chromosomes from different centromeric origin in a moderately mentally retarded male

    • J.R. Vermeesch
    • H. Duhamel
    • P. Marynen

    Original Investigation 04 November 1999 Pages: 611 - 618

14. Genes and chromosomal breakpoints in the Langer-Giedion syndrome region on human chromosome 8

    • H.-J. Lüdecke
    • O. Schmidt
    • B. Horsthemke

    Original Investigation 16 November 1999 Pages: 619 - 628

15. Germline origins in the human F9 gene: frequent G:C→A:T mosaicism and increased mutations with advanced maternal age

    • R.P. Ketterling
    • E. Vielhaber
    • S.S. Sommer

    Original Investigation 19 October 1999 Pages: 629 - 640

16. Genetic susceptibility to pre-eclampsia and chromosome 7q36

    • G. Guo
    • J.A. Lade
    • S.P. Brennecke

    Original Investigation 16 November 1999 Pages: 641 - 647

17. Novel mutations in the 3' region of the polycystic kidney disease 1 (PKD1) gene

    • A.R. Afzal
    • M. Hand
    • S. Jeffery

    Original Investigation 16 November 1999 Pages: 648 - 653

18. Inheritance of heart rate variability: the kibbutzim family study

    • R. Sinnreich
    • Y. Friedlander
    • J.D. Kark

    OriginalPaper 10 November 1999 Pages: 654 - 661

19. The EIF3S3 gene encoding the p40 subunit of the translation initiation factor eIF3 has eight exons and maps to the Langer-Giedion syndrome chromosome region on 8q24, but is not the TRPS1 gene

    • O. Schmidt
    • D. von Holtum
    • H.-J. Lüdecke

    Short Report 17 November 1999 Pages: 662 - 664

20. A 5-kb imprinting center deletion in a family with Angelman syndrome reduces the shortest region of deletion overlap to 880 bp

    • K. Buiting
    • C. Lich
    • B. Horsthemke

    Short Report 16 November 1999 Pages: 665 - 666

21. Letter to human genetics journals

    • Segolene Ayme

    Letter to the Editor 16 November 1999 Pages: 667 - 668