Molecular Diagnosis

Investigation into a Possible Association Between Oral Lichen Planus, the Human Herpesviruses, and the Human Papillomaviruses
pp. 73-83(11)
Authors: ÓFlatharta C.; Flint S.R.; Toner M.; Butler D.; Mabruk M.J.E.M.F.

Renewable Standard Reference Material for the Detection of TP53 Mutations
pp. 85-97(13)
Authors: O’Connell C.D.; Tully L.A.; Devaney J.M.; Marino M.A.; Jakupciak J.P.; Atha D.H.

C677T Single Nucleotide Polymorphisms of the Human Methylene Tetrahydrofolate Reductase and Specific Identification: A Novel Strategy Using Two-Color Cross-Correlation Fluorescence Spectroscopy
pp. 99-111(13)
Authors: Földes-Papp Z.; Kinjo M.; Saito K.; Kii H.; Takagi T.; Tamura M.; Costa J.M.; Birch-Hirschfeld E.; Demel U.; Thyberg P.; Tilz G.P.

Uniparental Disomy and Robertsonian Translocations: Risk Estimation and Prenatal Testing
pp. 113-117(5)
Authors: Eggermann T.; Zerres K.

Endothelial Nitric Oxide Synthase Gene Intron 4 Polymorphism in Type 2 Diabetes Mellitus
pp. 119-123(5)
Authors: Ksiazek P.; Wojewoda P.; Muc K.; Buraczynska M.

Hyperekplexia (Startle Disease): A Novel Mutation (S270T) in the M2 Domain of the GLRA1 Gene and a Molecular Review of the Disorder
pp. 125-128(4)
Authors: Lapunzina P.; Sánchez J.M.; Cabrera M.; Moreno A.; Delicado A.; de Torres M.L.; Mori A.M.; Quero J.; Pajares I.L.

A Novel Mutation in Exon 5 of the Glucokinase Gene in an Argentinian Family with Maturity Onset Diabetes of the Young
pp. 129-131(3)
Authors: Frechtel G.D.; López A.P.; Rodríguez M.; Cerrone G.E.; Targovnik H.M.