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International Journal of Human and Medical Genetics

Original Papers

Screening 25 Dystrophin Gene Exons for Deletions in Arab Children with Duchenne Muscular Dystrophy

Haider, M.Z.; Bastaki, L.; Habib, Y.; Moosa, A. (Safat)

A Conditional Inference Framework for Extending the Transmission/Disequilibrium Test

Lazzeroni, L.C. (Stanford, Calif.); Lange, K. (Ann Arbor, Mich.)

Fluorescence in situ Hybridization of psu dic(X)(Xpter-Xq21::Xq21-Xpter) in Two Patients with Turner's Syndrome

Fernández, R.; Pásaro, E. (La Coruña)

A Novel Missense Mutation in the DNA Mismatch Repair Gene hMLH1 Present among East Asians but Not among Europeans

Wang, Y.; Friedl, W.; Lamberti, C.; Nöthen, M.M.; Kruse, R.; Propping, P. (Bonn)

G6PD Variants in Three South American Ethnic Groups: Population Distribution and Description of Two New Mutations

Weimer, T.A.; Salzano, F.M. (Porto Alegre); Westwood, B.; Beutler, E. (La Jolla, Calif.)

Extreme Selection Strategies in Gene Mapping Studies of Oligogenic Quantitative Traits Do Not Always Increase Power

Allison, D.B.; Heo, M. (New York, N.Y.); Schork, N.J. (Cleveland, Ohio/Boston, Mass./Bar Harbor, Me.); Wong, S.-L. (New York, N.Y.); Elston, R.C. (Cleveland, Ohio)

Saami Mitochondrial DNA Reveals Deep Maternal Lineage Clusters

Delghandi, M. (Tromsø); Utsi, E. (Karasjok); Krauss, S. (Tromsø)

Methodological Issues

An Adenine Trimer Precedes a C/G Polymorphism in the 3’-Amplimer Region of the Human Platelet Glycoprotein IIIa Intron 6 CT Repeat

Denomme, G.A. (Hamilton/Toronto)

Mutation Report

A Novel Mutation Q602STOP in Exon 12 of the FVIII Gene

Strmecki, L.; Benedik-Dolnicar, M.; Komel, R. (Ljubljana)

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