1. Molecular pathology and evolutionary and physiological implications of pancreatitis-associated cationic trypsinogen mutations

   • Jian-Min Chen
   • Tristan Montier
   • Claude Férec

   Review Article 21 August 2001 Pages: 245 - 252

2. Extent of linkage disequilibrium between the androgen receptor gene CAG and GGC repeats in human populations: implications for prostate cancer risk

   • Rick A. Kittles
   • Dale Young
   • Georgia M. Dunston

   Original Investigation 04 August 2001 Pages: 253 - 261

3. Association between nasal allergy and a coding variant of the Fc ε RI β gene Glu237Gly in a Japanese population

   • H. Nagata
   • H. Mutoh
   • A. Konno

   Original Investigation 16 August 2001 Pages: 262 - 266

4. Compound heterozygosity and nonsense mutations in the α₁-subunit of the inhibitory glycine receptor in hyperekplexia

   • Mark I. Rees
   • Trevor M. Lewis
   • Michael J. Owen

   Original Investigation 02 August 2001 Pages: 267 - 270

5. DNA sequence comparison of human and mouse retinitis pigmentosa GTPase regulator (RPGR) identifies tissue-specific exons and putative regulatory elements

   • Renate Kirschner
   • Deniz Erturk
   • Wolfgang Berger

   Original Investigation 16 August 2001 Pages: 271 - 278

6. Linkage of body mass index to chromosome 20 in Utah pedigrees

   • Steven C. Hunt
   • Victor Abkevich
   • Steven Stone

   Original Investigation 21 August 2001 Pages: 279 - 285

7. Submicroscopic terminal deletions and duplications in retarded patients with unclassified malformation syndromes

   • Mariluce Riegel
   • Alessandra Baumer
   • Albert Schinzel

   Original Investigation 25 August 2001 Pages: 286 - 294

8. Absence of correlation between late-replication and spreading of X inactivation in an X;autosome translocation

   • Andrew Sharp
   • David O. Robinson
   • Patricia Jacobs

   Original investigation 16 August 2001 Pages: 295 - 302

9. Polymorphism in the alpha₁-antichymotrypsin (ACT) gene promoter: effect on expression in transfected glial and liver cell lines and plasma ACT concentrations

   • Kevin Morgan
   • Federico Licastro
   • Noor Kalsheker

   Original Investigation 22 August 2001 Pages: 303 - 310

10. Scanning for telomeric deletions and duplications and uniparental disomy using genetic markers in 120 children with malformations

    • M. Rosenberg
    • C. Killoran
    • L. Biesecker

    Original Investigation 31 July 2001 Pages: 311 - 318

11. Polymorphisms within the prion-like protein gene (Prnd) and their implications in human prion diseases, Alzheimer's disease and other neurological disorders

    • Björn Schröder
    • Bettina Franz
    • Inga Zerr

    Original Investigation 25 August 2001 Pages: 319 - 325

12. Mutational scanning of the ABCR gene with double-gradient denaturing-gradient gel electrophoresis (DG-DGGE) in Italian Stargardt disease patients

    • Antonella Fumagalli
    • Maurizio Ferrari
    • Laura Cremonesi

    Original Investigation 22 August 2001 Pages: 326 - 338

13. Genomic structures and population histories of linguistically distinct tribal groups of India

    • Susanta Roychoudhury
    • Sangita Roy
    • Partha P. Majumder

    Original Investigation 16 August 2001 Pages: 339 - 350

14. Respiratory distress syndrome: evaluation of genetic susceptibility and protection by transmission disequilibrium test

    • Ritva Haataja
    • Riitta Marttila
    • Mikko Hallman

    Original Investigation 09 August 2001 Pages: 351 - 355

15. Identification of ABCC6 pseudogenes on human chromosome 16p: implications for mutation detection in pseudoxanthoma elasticum

    • Leena Pulkkinen
    • Aoi Nakano
    • Jouni Uitto

    Original Investigation 22 August 2001 Pages: 356 - 365

16. Genetics and public health in the 21^st century

    • R. Skinner

    Book Review 25 August 2001 Pages: 366 - 367