Mutation analysis of the coding sequence of the MECP2 gene in infantile autism Kim S. BeyerFrancesca Blasi International Molecular Genetic Study of Autism Consortium (IMGSAC) Original Investigation Pages: 305 - 309
Evidence for differential S100 gene over-expression in psoriatic patients from genetically heterogeneous pedigrees Sabrina SempriniFrancesca CaponGiuseppe Novelli Original Investigation Pages: 310 - 313
Mutation analysis of five new patients affected by prolidase deficiency: the lack of enzyme activity causes necrosis-like cell death in cultured fibroblasts Antonella ForlinoAnna LupiGiuseppe Cetta Original Investigation Pages: 314 - 322
Periodic catatonia: confirmation of linkage to chromosome 15 and further evidence for genetic heterogeneity Gerald StöberDominik SeelowAndré Reis Original Investigation Pages: 323 - 330
Evidence for a founder effect for pseudoxanthoma elasticum in the Afrikaner population of South Africa Olivier Le SauxKonstanze BeckCharles D. Boyd Original Investigation Pages: 331 - 338
A detailed physical map of the 6p reading disability locus, including new markers and confirmation of recombination suppression Jung AhnTae-Woong WonJeffrey R. Gruen Original Investigation Pages: 339 - 349
Argininosuccinate lyase (ASL) deficiency: mutation analysis in 27 patients and a completed structure of the human ASL gene Michael LinnebankEva TschiedelHans G. Koch Original Investigation Pages: 350 - 359
Genetic basis of inosine triphosphate pyrophosphohydrolase deficiency Satoshi SumiAnthony M. MarinakiJohn A. Duley Original Investigation Pages: 360 - 367
A novel mutation in the IHH gene causes brachydactyly type A1: a 95-year-old mystery resolved Elizabeth M. McCreadyElizabeth SweeneyDennis E. Bulman Original Investigation Pages: 368 - 375
Chromosome 7p disruptions in Silver Russell syndrome: delineating an imprinted candidate gene region. David MonkLouise BentleyGudrun E. Moore Original Investigation Pages: 376 - 387
Identification of a novel SCA locus (SCA19) in a Dutch autosomal dominant cerebellar ataxia family on chromosome region 1p21-q21 Dineke S. VerbeekJurgen H. SchelhaasRichard J. Sinke Original Investigation Pages: 388 - 393
The prevalence of connexin 26 (GJB2) mutations in the Chinese population Xue LiuXia XiaLi Xu Original Investigation Pages: 394 - 397
ELAC2 and prostate cancer risk in Afro-Caribbeans of Tobago Patrick R. SheaRobert E. FerrellClareann H. Bunker Original Investigation Pages: 398 - 400
Assignment of a locus for autosomal dominant idiopathic scoliosis (IS) to human chromosome 17p11 Leila SalehiMassimo ManginoBruno Dallapiccola Original Investigation Pages: 401 - 404
Duplication of the CYP21A2 gene complicates mutation analysis of steroid 21-hydroxylase deficiency: characteristics of three unusual haplotypes Paul F. KoppensTheo HoogenboezemHerman J. Degenhart Original Investigation Pages: 405 - 410
Associations between gene expressions in breast cancer and patient survival T.-K. Jenssen W. Kuo E. Hovig Original Investigation Pages: 411 - 420
Absence of PTPN11 mutations in 28 cases of cardiofaciocutaneous (CFC) syndrome Andra IonMarco TartagliaSteve Jeffery Original Investigation Pages: 421 - 427
Linkage of one gene for familial glucocorticoid deficiency type 2 (FGD2) to chromosome 8q and further evidence of heterogeneity Emmanuelle GéninAngela HuebnerDanielle Naville Original Investigation Pages: 428 - 434
Identification and characterisation of novel mammalian homologues of Drosophila polyhomeotic permits new insights into relationships between members of the polyhomeotic family Emma TonkinDonna-Marie HaganTom Strachan Original Investigation Pages: 435 - 442
Investigation of oxidized LDL-receptor 1 (OLR1) as the candidate gene for Alzheimer's disease on chromosome 12 Erin Luedecking-ZimmerSteven T. DeKoskyIlyas M. Kamboh Original Investigation Pages: 443 - 451
CTLA-4 gene polymorphisms in systemic lupus erythematosus: a highly significant association with a determinant in the promoter region Lori L. HudsonKeith RoccaJanardan P. Pandey Original Investigation Pages: 452 - 455
A novel locus for Meckel-Gruber syndrome, MKS3, maps to chromosome 8q24 Neil V. MorganPaul GissenColin A. Johnson Original Investigation Pages: 456 - 461
Mitochondrial DNA 5178A polymorphism and longevity Yong-Gang YaoQing-Peng KongYa-Ping Zhang Short Report Pages: 462 - 463
Mutations in PATCHED-1, the receptor for SONIC HEDGEHOG, are associated with holoprosencephaly Jeffrey E. MingMichelle E. KaupasMaximilian Muenke Erratum Pages: 464 - 464
Molecular characterisation of t(17;22)(q11.2;q11.2) is not consistent with NF1 gene duplication Hildegard Kehrer-SawatzkiGünter AssumHorst Hameister Letter to the Editor Pages: 465 - 467
Genomic evidence versus characterisation of a single (17;22) translocation on NF1 gene duplication: lessons from deletions in "balanced" chromosomal rearrangements. Reply Paola RivaCristina GervasiniLidia Larizza Letter to the Editors Pages: 468 - 469
Frontiers of hormone research (series editor: A.B. Grossman), volume 28: genetic disorders of endocrine neoplasia Simon Pearce Book Review Pages: 472 - 472
Derek Chadwick, Jamie Goode (eds): The Genetics and Biology of Sex Determination (Novartis Symposium 244) Andy Greenfield Book Review Pages: 473 - 474
