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virtual library in human genetics and molecular biology

Original Papers
Mapping Genes for Polygenic Disorders: Considerations for Study Design in the Complex Trait of Inflammatory Bowel Disease
Hampe, J. (Kiel); Wienker, T. (Bonn); Nürnberg, P. (Berlin); Schreiber, S. (Kiel)

Fine Mapping of the Human Biotinidase Gene and Haplotype Analysis of Five Common Mutations
Blanton, S.H. (Charlottesville, Va./Richmond, Va.); Pandya, A.; Landa, B.L.; Javaheri, R.; Xia, X.-J.; Nance, W.E.; Pomponio, R.J.; Norrgard, K.J.; Swango, K.L. (Richmond, Va.); Demirkol, M.; Gülden, H. (Istanbul); Coskun, T.; Tokatli, A.; Ozalp, I. (Ankara); Wolf, B. (Richmond, Va.)

Allele-Specific Variation in the Gene Copy Number of Human Cytosine 5-Methyltransferase
Franchina, M.; Kay, P.H. (Perth)

alpha-Thalassemia in Bantu Population from Congo-Brazzaville: Its Interaction with Sickle Cell Anemia
Mouélé, R. (Créteil/Brazzaville); Pambou, O. (Brazzaville); Feingold, J. (Paris); Galactéros, F. (Créteil)

Effects of Misspecification of Allele Frequencies on the Type I Error Rate of Model-Free Linkage Analysis
Mandal, D.M. (New Orleans, La.); Wilson, A.F. (Baltimore, Md.); Elston, R.C. (Cleveland, Ohio); Weissbecker, K.; Keats, B.J. (New Orleans, La.); Bailey-Wilson, J.E. (Baltimore, Md.)

Methodological Issues
Model-Free Analysis and Permutation Tests for Allelic Associations
Zhao, J.H.; Curtis, D.; Sham, P.C. (London)

Mutation Report
A Novel Q562X Mutation Identified in the hMLH1 Gene in a Slovenian Patient with Hereditary Nonpolyposis Colorectal Cancer
Potocnik, U.; Glavac , D.; Golouh, R.; Ravnik-Glavac , M. (Ljubljana)

Case Report
Cystic Fibrosis Mutations: Report from the French Registry
Guilloud-Bataille, M.; De Crozes, D. (Paris); Rault, G. (Roscoff); Degioanni, A.; Feingold, J.; The Clinical Centers of the CF French Registry (Paris)

Clinical Report
A New Inherited Interstitial Deletion of the Distal Long Arm of Chromosome 4,{del(4)(q32 q33)}
Aladhami, S.M.S. (Warwick); Gould, C.P. (Birmingham); Muhammad, F.A. (Glasgow)

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