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American Journal of Medical Genetics|April 1, 1992
Collaborative prospective study of the fragile X syndrome: one-year progress reportS L Sherman, G Barbi, K Brøndum-Nielsen, et al.
Human Molecular Genetics|June 1, 1992
Molecular analysis of patients with Hunter syndrome: implication of a region prone to structural alterations within the IDS geneM L Steén-Bondeson, N Dahl, T Tönnesen, et al.
American Journal of Medical Genetics|February 1, 1991
Guidelines for the preparation and analysis of the fragile X chromosome in lymphocytesP B Jacky, Y R Ahuja, K Anyane-Yeboa, et al.
Annals of Neurology|February 16, 1999
Friedreich's ataxia: point mutations and clinical presentation of compound heterozygotesM Cossée, A Dürr, M Schmitt, et al.
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