Friedreich's ataxia phenotype not linked to chromosome 9 and associated with selective autosomal recessive vitamin E deficiency in two inbred Tunisian families
Ben Hamida, M, Belal, S, Sirugo, G, Ben Hamida, C, Panayides, K, Ionannou, P, Beckmann, J, Mandel, J L, Hentati, F, Koenig, M
Published in Neurology (01.11.1993)
Published in Neurology (01.11.1993)
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Journal Article
Study of large inbred Friedreich ataxia families reveals a recombination between D9S15 and the disease locus
BELAL, S, PANAYIDES, K, MIDDLETON, L. T, SIRUGO, G, BEN HAMIDA, C, IOANNOU, P, HENTATI, F, BECKMANN, J, KOENIG, M, MANDEL, J.-L, MONGI BEN HAMIDA
Published in American journal of human genetics (01.12.1992)
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Published in American journal of human genetics (01.12.1992)
Journal Article
An integrated system for medical diagnosis: Laboratory findings
Pattichis, C. S., Fredj, M., Schizas, C. N., Gabriel, G., Panayides, K., Drousiotou, A., Livesay, R. R., Middleton, L. T.
Published in 1992 14th Annual International Conference of the IEEE Engineering in Medicine and Biology Society (01.10.1992)
Published in 1992 14th Annual International Conference of the IEEE Engineering in Medicine and Biology Society (01.10.1992)
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