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Original Papers

True Pedigree Errors More Frequent Than Apparent Errors for Single Nucleotide Polymorphisms
Gordon, D.; Heath, S.C.; Ott, J. (New York, N.Y.)

Molecular Genetic Study of Autosomal Dominant Retinitis pigmentosa in Lithuanian Patients
Kucinskas, V. (Vilnius); Payne, A.M. (London); Ambrasiene., D.; Jurgelevicius, V.; Steponaviciute., D. (Vilnius); Arciuliene., J.V.; Daktaraviciene., E. (Kaunas); Bhattacharya, S. (London)

Human NDUFB9 Gene: Genomic Organization and a Possible Candidate Gene Associated with Deafness Disorder Mapped to Chromosome 8q13
Lin, X.; Wells, D.E. (Houston, Tex.); Kimberling, W.J.; Kumar, S. (Omaha, Nebr.)

Analysis of the Complete Coding Region of the CFTR Gene in Ten Algerian Cystic Fibrosis Families
Loumi, O.; Baghriche, M. (Alger); Delpech, M.; Kaplan, J.C.; Bienvenu, T. (Paris)

Contribution of Interleukin 1beta and KM Loci to Alopecia areata
Galbraith, G.M.P.; Palesch, Y.; Gore, E.A.; Pandey, J.P. (Charleston, S.C.)

Linkage Disequilibrium and Haplotype Analysis in German Friedreich Ataxia Families
Zühlke, C.; Gehlken, U.; Purmann, S.; Kunisch, M. (Lübeck); Müller-Myhsok, B. (Hamburg); Kreuz, F. (Dresden); Laccone, F. (Göttingen)

Hereditary Desmoid Disease in a Family with a Germline Alu I Repeat Mutation of the APC Gene
Halling, K.C. (Indianapolis, Ind./Rochester, Minn.); Lazzaro, C.R.; Honchel, R. (Indianapolis, Ind.); Bufill, J.A. (Elkhart, Ind.); Powell, S.M. (Charlottesville, Va.); Arndt, C.A.S.; Lindor, N.M. (Rochester, Minn.)

No Correlation between A(–1438)G Polymorphism in 5-HT2A Receptor Gene Promoter and the Density of Frontal Cortical 5-HT2A Receptors in Schizophrenia
Kouzmenko, A.P.; Scaffidi, A.; Pereira, A.M.; Hayes, W.L.; Copolov, D.L.; Dean, B. (Parkville)

A Principal-Components Approach Based on Heritability for Combining Phenotype Information
Ott, J.; Rabinowitz, D. (New York, N.Y.)

Linkage Information Content of Polymorphic Genetic Markers
Guo, X.; Elston, R.C. (Cleveland, Ohio)


Mutation Reports

A Novel Splice Site Mutation in a Brazilian Patient with Hereditary Antithrombin Deficiency Type I
Arnaldi, L. A.T. (Campinas); Polimeno, N.C. (Bragança Paulista); Arruda, V.R.; Annichino-Bizzacchi, J.M. (Campinas)

A Novel Nonsense Mutation 6, E – X in the Protein S Gene Causes Type I Deficiency
Pugliese, L.; Arruda, V.R.; Annichino-Bizzacchi, J.M. (São Paulo)

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