1. Linkage and association mapping of the LRP5 locus on chromosome 11q13 in type 1 diabetes

   • Rebecca C. J. Twells
   • Charles A. Mein
   • John A. Todd

   Original Investigation 17 April 2003 Pages: 99 - 105

   

2. ABCA1 gene polymorphisms and their associations with coronary artery disease and plasma lipids in males from three ethnic populations in Singapore

   • Jenny Hui-Hui Tan
   • Poh-Sim Low
   • Chew-Kiat Heng

   Original Investigation 23 April 2003 Pages: 106 - 117

   

3. A deletion in the human QP-C gene causes a complex III deficiency resulting in hypoglycaemia and lactic acidosis

   • Sandrine Haut
   • Michèle Brivet
   • Abdelhamid Slama

   Original Investigation 23 April 2003 Pages: 118 - 122

   

4. Common 5′ β-globin RFLP haplotypes harbour a surprising level of ancestral sequence mosaicism

   • Matthew T. Webster
   • John B. Clegg
   • Rosalind M. Harding

   Original Investigation 08 May 2003 Pages: 123 - 139

   

5. Disruption of exon definition produces a dominant-negative growth hormone isoform that causes somatotroph death and IGHD II

   • Robin C. C. Ryther
   • Lindsay M. McGuinness
   • James G. Patton

   Original Investigation 29 April 2003 Pages: 140 - 148

   

6. Cis-acting variation in the expression of a high proportion of genes in human brain

   • Nicholas J. Bray
   • Paul R. Buckland
   • Michael C. O'Donovan

   Original Investigation 01 May 2003 Pages: 149 - 153

   

7. Translocation breakpoint in two unrelated Tourette syndrome cases, within a region previously linked to the disorder

   • Fiona C. Crawford
   • Ghania Ait-Ghezala
   • Michael J. Mullan

   Original Investigation 16 April 2003 Pages: 154 - 161

   

8. Mucopolysaccharidosis IVA: characterization of a common mutation found in Finnish patients with attenuated phenotype

   • Adriana Maria Montaño
   • Ilkka Kaitila
   • Naomi Kondo

   Original Investigation 30 April 2003 Pages: 162 - 169

   

9. SONIC HEDGEHOG mutations causing human holoprosencephaly impair neural patterning activity

   • Can Schell-Apacik
   • Mariel Rivero
   • Jeffrey E. Ming

   Original Investigation 23 April 2003 Pages: 170 - 177

   

10. Hyaluronan is not elevated in urine or serum in Hutchinson-Gilford Progeria Syndrome

    • Leslie B. Gordon
    • Ingrid A. Harten
    • Bryan P. Toole

    Original Investigation 01 May 2003 Pages: 178 - 187

    

11. Interphase FISH, the structure of reciprocal translocation chromosomes and physical mapping studies rule out the duplication of the NF1 gene at 17q11.2. A reply

    • Hildegard Kehrer-Sawatzki
    • Ludwine Messiaen

    Letter to the Editor 16 April 2003 Pages: 188 - 190

    

12. Methods in molecular biology, vol 204. Molecular cytogenetics: protocols and applications

    • John A. Crolla

    Book Review 23 April 2003 Pages: 191 - 192

13. David J. Galas, Stephen J. McCormack (eds): Genomic Technologies — Present and Future. Functional Genomics Series, Vol 1 (Series ed: Milton H. Saier Jr)

    • Paul Dear

    Book Review 13 May 2003 Pages: 193 - 193

14. Bone dysplasias: an atlas of genetic disorders of skeletal development, 2nd edition

    • Ian D. Young

    Book Review 23 April 2003 Pages: 194 - 194