Thank you Robert Nussbaum, Welcome Thomas Hudson! Rolf Lange Editorial 05 February 2003 Pages: 219 - 219
The novel imprinted carboxypeptidase A4 gene (CPA4) in the 7q32 imprinting domain Tomohiko KayashimaKentaro YamasakiTatsuya Kishino Original Investigation 28 January 2003 Pages: 220 - 226
Assessment of the CTNNA3 gene encoding human αT-catenin regarding its involvement in dilated cardiomyopathy Barbara JanssensBhagyalaxmi MohapatraJeffrey A. Towbin Original Investigation Pages: 227 - 236
Influence of interleukin-12 receptor β1 polymorphisms on tuberculosis Mitsuteru AkahoshiHitoshi NakashimaMine Harada Original Investigation 13 December 2002 Pages: 237 - 243
Founder effect of the C9 R95X mutation in Orientals Vahid KhajoeeKenji IharaToshiro Hara Original Investigation 09 January 2003 Pages: 244 - 248
Duplication of the MID1 first exon in a patient with Opitz G/BBB syndrome Jennifer WinterTanja LehmannSusann Schweiger Original Investigation 24 January 2003 Pages: 249 - 254
Testing hypotheses of language replacement in the Caucasus: evidence from the Y-chromosome Ivan NasidzeTamara SarkisianMark Stoneking Original Investigation 14 December 2002 Pages: 255 - 261
FMR1 haplotype analyses among Indians: a weak founder effect and other findings Deepti SharmaMeena GuptaB. K. Thelma Original Investigation 14 December 2002 Pages: 262 - 271
Relevance of sequence and structure elements for deletion events in the dystrophin gene major hot-spot Manuela SironiUberto PozzoliNereo Bresolin Original Investigation 19 December 2002 Pages: 272 - 288
Patterns of associations of clinical features in neurofibromatosis 1 (NF1) Jacek SzudekD. Gareth EvansJan M. Friedman Original Investigation 20 December 2002 Pages: 289 - 297
A study of cryptic terminal chromosome rearrangements in recurrent miscarriage couples detects unsuspected acrocentric pericentromeric abnormalities Annette E. CockwellPatricia A. JacobsJohn A. Crolla Original Investigation 08 January 2003 Pages: 298 - 302
Human genetic disease caused by de novo mitochondrial-nuclear DNA transfer Clesson TurnerChristina KilloranLeslie G. Biesecker Original Investigation 25 January 2003 Pages: 303 - 309
Relation of risk of systemic lupus erythematosus to west African admixture in a Caribbean population M. MolokhiaC. HoggartP. M. McKeigue Original Investigation 24 January 2003 Pages: 310 - 318
A novel autosomal dominant non-syndromic deafness locus (DFNA48) maps to 12q13-q14 in a large Italian family Pio D'AdamoMaura PinnaPaolo Gasparini Short Report 13 December 2002 Pages: 319 - 320
Helen M. Kingston: ABC of Clinical Genetics (3rd edn) Julia Rankin Book Review 18 January 2003 Pages: 321 - 321
Frederick Burkhardt, Duncan M. Porter, Sheila Ann Dean, Jonathan R. Topham, Sarah Wilmot (eds): The Correspondence of Charles Darwin 1864 (Vol. 12) Peter Harper Book Review 15 January 2003 Pages: 322 - 322
Fragile X syndrome: diagnosis, treatment and research Bert B. A. de Vries Book Review 25 January 2003 Pages: 323 - 323