European Journal of Human Genetics: Vol. 4, No. 4, 1996 (July-August)

Original Papers

191 Evidence for a Common Origin of Most Friedreich Ataxia Chromosomes in the Spanish Population

Monrós, E.; Cañizares, J.; Moltó, M.D.; Rodius, F.; Montermini, L.; Cossée, M.; Martínez, F.; Prieto, F.; de Frutos, R.; Koenig, M.; Pandolfo, M.; Bertranpetit, J.; Palau, F. (Valènica/Houston, Tex./Strasbourg/Barcelona)

199 Assignment of Genes Encoding GABAA Receptor Subunits alpha1 , alpha6, ß2, and y2 to a YAC Contig of 5q33

Kostrzewa, M.; Köhler, A.; Eppelt, K.; Hellam, L.; Fairweather, N.D.; Levy, E.R.; Monaco, A.P.; Müller, U. (Giessen/Oxford)

205 Relative Frequency, Heterogeneity and Geographic Clustering of PKU Mutations in Norway

Eiken, H.G.; Knappskog, P.M.; Boman, H.; Thune, K.S.; Kaada, G.; Motzfeldt, K.; Apold, J. (Bergen/Oslo)

214 Delineation of a 1-cM Region on Distal 5q Containing the Locus for Corneal Dystrophies Groenouw Type I and Lattice Type I and Exclusion of the Candidate Genes SPARC and LOX

Korvatska, E.; Munier, F.L.; Zografos, L.; Ahmad, F.; Faggioni, R.; Dolivo-Beuret, A.; Uffer, S.; Pescia, G.; Schorderet, D.F. (Lausanne)

219 Fabry Disease: Fourteen alpha-Galactosidase A Mutations in Unrelated Families from the United Kingdom and Other European Countries

Davies, J.P.; Eng, C.M.; Hill, J.A.; Malcolm, S.; MacDermot, K.; Winchester, B.; Desnick, R.J. (London/New York, N.Y.)

225 The Majority of 22 Dutch High-Risk Breast Cancer Families Are due to Either BRCA1 or BRCA2

Peelen, T.; Cornelis, R.S.; van Vliet, M.; Petrij-Bosch, A.; Cleton-Jansen, A.-M.; Meijers-Heijboer, H.; Klijn, J.G.M.; Vasen, H.F.A.; Cornelisse, C.J.; Devilee, P. (Leiden/Rotterdam)

231 Prenatal Prediction of Spinal Muscular Atrophy. Experience with Linkage Studies and Consequences of Present SMN Deletion Analysis

Cobben, J.M.; Scheffer, H.; De Visser, M.; Van der Steege, G.; Verhey, J.B.B.M.; Osinga, J.; Burton, M.; Mensink, R.G.J.; Grootscholten, P.M.; Ten Kate, L.P.; Buys, C.H.C.M. (Groningen/Amsterdam)

Short Reports

237 Assignment of Genes Coding for Brown Eye Colour (BEY2) and Brown Hair Colour (HCL3) on Chromosome 15q

Eiberg, H.; Mohr, J. (Copenhagen)

242 A High-Resolution Radiation Hybrid Map of the Region Surrounding the Gorlin Syndrome Gene

Obermayr, F.; Walter, M.A.; Jones, H.B.; Goodfellow, P.N.; Frischauf, A.-M. (London/Cambridge/Edmonton)

246 Announcement