A genome-wide search for genes predisposing to familial psoriasis by using a stratification approach L. SamuelssonF. EnlundT. Martinsson Original Investigation 04 November 1999 Pages: 523 - 529
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. OsipovaO.L. PosukhM.-P. Lefranc Original Investigation 17 November 1999 Pages: 530 - 541
Association between monoamine oxidase A activity in human male skin fibroblasts and genotype of the MAOA promoter-associated variable number tandem repeat R.M. DenneyH. KochI.W. Craig Original Investigation 04 November 1999 Pages: 542 - 551
A novel gene containing LIM domains (LIMD1) is located within the common eliminated region 1 (C3CER1) in 3p21.3 H. KissD. KedraJ.P. Dumanski Original Investigation 17 November 1999 Pages: 552 - 559
Two novel mutations of SURF1 in Leigh syndrome with cytochrome c oxidase deficiency M. TeraokaY. YokoyamaY. Seino Original Investigation 16 November 1999 Pages: 560 - 563
Correlation between human papillomavirus-associated cervical cancer and p53 codon 72 arginine/proline polymorphism R. TachezyI. MikyškováM. Van Ranst Original Investigation 23 October 1999 Pages: 564 - 566
Minisatellite mutational processes reduce Fst estimates J. FlintJ. BondR. M. Harding Original Investigation 05 November 1999 Pages: 567 - 576
High throughput analysis of 10 microsatellite and 11 diallelic polymorphisms on the human Y-chromosome M.G. ThomasN. BradmanH.M. Flinn Original Investigation 04 November 1999 Pages: 577 - 581
Genomic characterization of the human peptidyl-prolyl-cis-trans-isomerase, mitochondrial precursor gene: assessment of its role in familial dilated cardiomyopathy K.R. BowlesC. ZintzJ.A. Towbin Original Investigation 26 October 1999 Pages: 582 - 586
Molecular analysis of eight mutations in FBN1 D. HallidayS. HutchinsonP. A. Handford Original Investigation 17 November 1999 Pages: 587 - 597
Screening for UBE3A gene mutations in a group of Angelman syndrome patients selected according to non-stringent clinical criteria A. BaumerD. BalmerA. Schinzel Original Investigation 16 November 1999 Pages: 598 - 602
MEN I gene mutations in sporadic adrenal adenomas K.-M. SchulteM. HeinzeH.-D. Röher Original Investigation 16 November 1999 Pages: 603 - 610
Multiple small accessory marker chromosomes from different centromeric origin in a moderately mentally retarded male J.R. VermeeschH. DuhamelP. Marynen Original Investigation 04 November 1999 Pages: 611 - 618
Genes and chromosomal breakpoints in the Langer-Giedion syndrome region on human chromosome 8 H.-J. LüdeckeO. SchmidtB. Horsthemke Original Investigation 16 November 1999 Pages: 619 - 628
Germline origins in the human F9 gene: frequent G:C→A:T mosaicism and increased mutations with advanced maternal age R.P. KetterlingE. VielhaberS.S. Sommer Original Investigation 19 October 1999 Pages: 629 - 640
Genetic susceptibility to pre-eclampsia and chromosome 7q36 G. GuoJ.A. LadeS.P. Brennecke Original Investigation 16 November 1999 Pages: 641 - 647
Novel mutations in the 3' region of the polycystic kidney disease 1 (PKD1) gene A.R. AfzalM. HandS. Jeffery Original Investigation 16 November 1999 Pages: 648 - 653
Inheritance of heart rate variability: the kibbutzim family study R. SinnreichY. FriedlanderJ.D. Kark OriginalPaper 10 November 1999 Pages: 654 - 661
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. SchmidtD. von HoltumH.-J. Lüdecke Short Report 17 November 1999 Pages: 662 - 664
A 5-kb imprinting center deletion in a family with Angelman syndrome reduces the shortest region of deletion overlap to 880 bp K. BuitingC. LichB. Horsthemke Short Report 16 November 1999 Pages: 665 - 666
Letter to human genetics journals Segolene Ayme Letter to the Editor 16 November 1999 Pages: 667 - 668
