1. DNA hypermethylation: when tumour suppressor genes go silent

   • George A. Garinis
   • George P. Patrinos
   • Panayiotis G. Menounos

   Review 16 July 2002 Pages: 115 - 127

2. Major gene evidence after MTHFR-segregation analysis of serum homocysteine in families of patients undergoing coronary arteriography

   • Sun Jee
   • Kyung Song
   • Terri H. Beaty

   Original Investigation 29 June 2002 Pages: 128 - 135

3. FOXP2: novel exons, splice variants, and CAG repeat length stability

   • Heather A. Bruce
   • Russell L. Margolis

   Original Investigation 16 July 2002 Pages: 136 - 144

4. Progressive hearing loss, and recurrent sudden sensorineural hearing loss associated with GJB2 mutations – phenotypic spectrum and frequencies of GJB2 mutations in Austria

   • Andreas R. Janecke
   • Almut Hirst-Stadlmann
   • Doris Nekahm-Heis

   Original Investigation 03 July 2002 Pages: 145 - 153

5. Functional characterization of the new human GABA_A receptor mutation β3(R192H)

   • Andreas Buhr
   • Matt T. Bianchi
   • Erwin Sigel

   Original Investigation 16 July 2002 Pages: 154 - 160

6. Unexpectedly high prevalence of the mild form of propionic acidemia in Japan: presence of a common mutation and possible clinical implications

   • Tohru Yorifuji
   • Masahiko Kawai
   • Tatsutoshi Nakahata

   Original Investigation 04 July 2002 Pages: 161 - 165

7. Androgen receptor CAG polymorphism and prostate cancer risk

   • Nina Mononen
   • Tarja Ikonen
   • Johanna Schleutker

   Original Investigation 03 July 2002 Pages: 166 - 171

8. Evolution of a VNTR located within the promoter region of the thiopurine methyltransferase gene: inferences from population and sequence data

   • Sandra Alves
   • António Amorim
   • Maria Prata

   Original Investigation 16 July 2002 Pages: 172 - 178

9. Organization of the human liver carnitine palmitoyltransferase 1 gene (CPT1A) and identification of novel mutations in hypoketotic hypoglycaemia

   • Stéphanie Gobin
   • Jean-Paul Bonnefont
   • Laure Thuillier

   Original Investigation 16 July 2002 Pages: 179 - 189

10. Human connexin26 (GJB2) deafness mutations affect the function of gap junction channels at different levels of protein expression.

    • Eva Thönnissen
    • Raquel Rabionet
    • Thomas Ott

    Original Investigation 22 June 2002 Pages: 190 - 197

11. SOX10 mutations in chronic intestinal pseudo-obstruction suggest a complex physiopathological mechanism

    • Véronique Pingault
    • Mathilde Girard
    • Michel Goossens

    Original Investigation 06 July 2002 Pages: 198 - 206

12. Evidence for a gene influencing heart rate on chromosome 4 among hypertensives

    • Jemma B. Wilk
    • Richard H. Myers
    • Curtis R. Ellison

    Original Investigation 16 July 2002 Pages: 207 - 213

13. Megalencephalic leukoencephalopathy with subcortical cysts; a founder effect in Israeli patients and a higher than expected carrier rate among Libyan Jews

    • Bruria Ben-Zeev
    • Etgar Levy-Nissenbaum
    • Elon Pras

    Original Investigation 16 July 2002 Pages: 214 - 218

14. Functional characterization of a natural variant of luteinizing hormone

    • W. Liao
    • H. Goh
    • A. Roy

    Original Investigation 16 July 2002 Pages: 219 - 224

15. A life of Sir Francis Galton. From African exploration to the birth of eugenics

    • Peter S. Harper

    Book Review 29 June 2002 Pages: 225 - 225

16. Psychosocial genetic counseling

    • Christin L. Evans

    Book Review 10 July 2002 Pages: 226 - 226

17. Simopoulos AP, Pavlou KN (eds): Nutrition and fitness: Diet, genes, physical activity and health. World review of nutrition and dietetics, vol 89

    • Darren Schickle

    Book Review 16 July 2002 Pages: 227 - 228

18. Alan R. Clarke (ed): Transgenesis techniques — principles and protocols, 2nd edn.

    • Franz Theuring

    Book Review 19 July 2002 Pages: 229 - 230