1. Molecular genetic advances in tuberous sclerosis

   • Jeremy P. Cheadle
   • Mary Pat Reeve
   • David J. Kwiatkowski

   Review Article 11 August 2000 Pages: 97 - 114

2. Autosomal dominant polycystic kidney disease: molecular genetics and molecular pathogenesis

   • Michael Koptides
   • C. Constantinou Deltas

   Review Article 01 August 2000 Pages: 115 - 126

3. Genomic structure of a copy of the human TPTE gene which encompasses 87 kb on the short arm of chromosome 21

   • Michel Guipponi
   • Marie-Laure Yaspo
   • Stylianos E. Antonarakis

   Original Investigation 01 August 2000 Pages: 127 - 131

4. Genetic background of apparently idiopathic sporadic cerebellar ataxia

   • Ludger Schöls
   • Sandra Szymanski
   • Olaf Riess

   Original Investigation 03 August 2000 Pages: 132 - 137

5. Association of a variant in exon 31 of the sulfonylurea receptor 1 (SUR1) gene with type 2 diabetes mellitus in French Caucasians

   • André F. Reis
   • Wei-Zhen Ye
   • Gilberto Velho

   Original Investigation 11 August 2000 Pages: 138 - 144

6. Mutations in short stature homeobox containing gene (SHOX) in dyschondrosteosis but not in hypochondroplasia

   • Giedre Grigelioniene
   • Ole Eklöf
   • Lars Hagenäs

   Original Investigation 01 August 2000 Pages: 145 - 149

7. Porphobilinogen deaminase gene in African and Afro-Caribbean ethnic groups: mutations causing acute intermittent porphyria and specific intragenic polymorphisms

   • A.M. Robreau-Fraolini
   • H. Puy
   • J.C. Deybach

   Original Investigation 21 July 2000 Pages: 150 - 159

8. Immature end-plates and utrophin deficiency in congenital myasthenic syndrome caused by ε-AChR subunit truncating mutations

   • Jörn P. Sieb
   • Simone Kraner
   • Ortrud K. Steinlein

   Original Investigation 11 August 2000 Pages: 160 - 164

9. Characterization of TH1 and CTSZ, two non-imprinted genes downstream of GNAS1 in chromosome 20q13

   • David T. Bonthron
   • Bruce E. Hayward
   • Lisa Strain

   Original Investigation 10 August 2000 Pages: 165 - 175

10. Identification of missense, nonsense, and deletion mutations in the GRHPR gene in patients with primary hyperoxaluria type II (PH2)

    • Kylie E. Webster
    • Patrick M. Ferree
    • Scott D. Cramer

    Original Investigation 10 August 2000 Pages: 176 - 185

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

    • Qing Gao
    • Gail Tomlinson
    • Olufunmilayo I. Olopade

    Original Investigation 14 April 2000 Pages: 186 - 191

12. Protein truncating BRCA1 and BRCA2 mutations in African women with pre-menopausal breast cancer

    • Olufunmilayo I. Opolade
    • Qing Gao
    • Adeyinka G. Falusi

    Short Report 16 August 2000 Pages: 192 - 194

13. Detection of the fragile X syndrome protein for the evaluation of FMR1 intermediate alleles

    • Sergi Castellví-Bel
    • Miguel Fernández-Burriel
    • Montserrat Milà

    Short Report 01 August 2000 Pages: 195 - 196

14. Genetic association studies of bronchial asthma – a need for Bonferroni correction?

    • Michael Krawczak
    • Stefan Boehringer
    • Jörg T. Epplen

    Letter to the Editors 16 August 2000 Pages: 197 - 197