1. Linkage and association to candidate regions in Swedish atopic dermatitis families

   • Cilla Söderhäll
   • Maria Bradley
   • Magnus Nordenskjöld

   Original Investigation Pages: 129 - 135

2. The polyglutamine motif is highly conserved at the Clock locus in various organisms and is not polymorphic in humans

   • Quasar Saleem
   • Anuranjan Anand
   • Samir K. Brahmachari

   Original Investigation Pages: 136 - 142

3. Recombination in the pseudoautosomal region in a 47,XYY male

   • Renée H. Martin
   • Qinghua Shi
   • Leigh L. Field

   Original Investigation Pages: 143 - 145

4. Opposite association of two PPARG variants with cancer: overrepresentation of H449H in endometrial carcinoma cases and underrepresentation of P12A in renal cell carcinoma cases

   • Wendy M. Smith
   • Xiao-Ping Zhou
   • Charis Eng

   Original Investigation Pages: 146 - 151

5. AcroM fluorescent in situ hybridization analyses of marker chromosomes

   • Sabine Langer
   • Christine Fauth
   • Michael R. Speicher

   Original Investigation Pages: 152 - 158

6. Mutation analyses in 17 patients with deficiency in acid β-galactosidase: three novel point mutations and high correlation of mutation W273L with Morquio disease type B

   • Eduard Paschke
   • Ivica Milos
   • B. Radeva

   Original Investigation Pages: 159 - 166

7. The position of t(11;22)(q23;q11) constitutional translocation breakpoint is conserved among its carriers

   • I. Tapia-Páez
   • M. Kost-Alimova
   • J. Dumanski

   Original Investigation Pages: 167 - 177

8. Expression pattern, genomic structure and evaluation of the human SLC30A4 gene as a candidate for acrodermatitis enteropathica

   • Sébastien Küry
   • Marie-Claire Devilder
   • Jean-Paul Moisan

   Original Investigation Pages: 178 - 185

9. Identification and characterization of a tissue-specific silencer element in the first intron of the human acid maltase gene

   • Bo Yan
   • Nina Raben
   • Paul H. Plotz

   Original Investigation Pages: 186 - 190

10. Combined segregation-linkage analysis of plasma thrombin activatable fibrinolysis inhibitor (TAFI) antigen levels with TAFI gene polymorphisms

    • D.-A. Trégouet
    • H. Aubert
    • L. Tiret

    Original Investigation Pages: 191 - 197

11. Archival, demographic and genetic studies define a Sardinian sub-isolate as a suitable model for mapping complex traits

    • Andrea Angius
    • Paola M. Melis
    • Mario Pirastu

    Original Investigation Pages: 198 - 209

12. Large-scale molecular screening for galactosemia alleles in a pan-ethnic population

    • Makoto Suzuki
    • Carol West
    • Ernest Beutler

    Original Investigation Pages: 210 - 215

13. Germ line insertion of mtDNA at the breakpoint junction of a reciprocal constitutional translocation

    • Joan E. Willett-Brozick
    • Shazia A. Savul
    • Bora E. Baysal

    Original Investigation Pages: 216 - 223

14. The Basques according to polymorphic Alu insertions

    • M. de Pancorbo
    • M. López-Martínez
    • R. Herrera

    Original Investigation Pages: 224 - 233

15. A second case of somatic triple mosaicism in the CYBB gene causing chronic granulomatous disease

    • Deborah Noack
    • Paul G. Heyworth
    • Andrew R. Cross

    Original Investigation Pages: 234 - 238

16. Prevalence of BRCA1 and BRCA2 mutations among clinic-based African American families with breast cancer

    • Qing Gao
    • Gail Tomlinson
    • Olufunmilayo I. Olopade

    Erratum Pages: 239 - 240