Canine cystinuria: polymorphism in the canine SLC3A1 gene and identification of a nonsense mutation in cystinuric Newfoundland dogs Paula HenthornJunlong LiuUrs Giger Original Investigation Pages: 295 - 303
Molecular definition of Xq common-deleted region in patients affected by premature ovarian failure Anna MarozziEmanuela ManfrediniLeda Dalprà Original Investigation Pages: 304 - 311
Alu insertion polymorphisms in NW Africa and the Iberian Peninsula: evidence for a strong genetic boundary through the Gibraltar Straits David ComasFrancesc CalafellAntti Sajantila Original Investigation Pages: 312 - 319
Molecular and clinical analysis of Japanese patients with 3-hydroxy-3-methylglutaryl CoA lyase (HL) deficiency Junko MuroiTohru YorifujiTatsutoshi Nakahata Original investigation Pages: 320 - 326
Molecular analysis of the genotype-phenotype relationship in factor VII deficiency D. MillarG. Kemball-CookD. Cooper Original Investigation Pages: 327 - 342
Age- and tissue-specific variation of X chromosome inactivation ratios in normal women Andrew SharpDavid RobinsonPatricia Jacobs Original Investigation Pages: 343 - 349
Molecular analysis of the TSC1 and TSC2 tumour suppressor genes in sporadic glial and glioneuronal tumours Lee ParryJulie MaynardJeremy Cheadle Original Investigation Pages: 350 - 356
Allelic loss at the neurofibromatosis type 1 (NF1) gene locus is frequent in desmoplastic neurotropic melanoma Ralf GutzmerRudolf HerbstJürgen Weiss Original investigation Pages: 357 - 361
Changes in primary DNA sequence complexity influence the phenotypic consequences of mutations in human gene regulatory regions Michael KrawczakNadia ChuzhanovaDavid Cooper Original Investigation Pages: 362 - 365
Neurofibromatosis type 2 attributable to gonosomal mosaicism in a clinically normal mother, and identification of seven novel mutations in the NF2 gene Roberta SestiniRossella VivarelliLaura Papi Original Investigation Pages: 366 - 371
Analysis of HPC1, HPCX, and PCaP in Icelandic hereditary prostate cancer Jon BergthorssonGudrun JohannesdottirRosa Barkardottir Original Investigation Pages: 372 - 375
Components of the human spindle checkpoint control mechanism localize specifically to the active centromere on dicentric chromosomes Richard SafferyDanielle IrvineK. Choo Original Investigation Pages: 376 - 384
In-frame deletions of BRCA1 may define critical functional domains Elizabeth RohlfsChristine ChungLawrence Silverman Original Investigation Pages: 385 - 390
Apolipoprotein-E dependent role for the FAS receptor in early onset Alzheimer's disease: finding of a positive association for a polymorphism in the TNFRSF6 gene Lars FeukJonathan PrinceAnthony Brookes Original Investigation Pages: 391 - 396
Genomic structure of the human Ah receptor nuclear translocator gene (hARNT) Julia ScheelDieter Schrenk Short Report Pages: 397 - 399
Gene rearrangement on 1q21 introducing a duplication of the glucocerebrosidase pseudogene and a metaxin fusion gene Nahid TayebiJoseph ParkEllen Sidransky Short Report Pages: 400 - 403
Absence of trabecular meshwork-inducible stretch response (TISR)/oculomedin gene and proximal promoter mutation in primary open angle glaucoma patients Y.F. LeungL. BaumC.P. Pang Short Report Pages: 404 - 405
Characterization of the γc chain among 27 unrelated Japanese patients with X-linked severe combined immunodeficiency (X-SCID) Satoru KumakiNaoto IshiiShigeru Tsuchiya Short Report Pages: 406 - 408