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Authors: Middleton-Price, H. R. Harding, A. E. Monteiro, C. Berciano, I. Malcolm, S.
Citation: R. Middleton-price, H. et al., Linkage of hereditary motor and sensory neuropathy type I to the pericentromeric region of chromosome 17, American journal of human genetics , 46-I(1), 1990, pp. 92-94

Authors: Holt, I. J. Harding, A. E. Petty, R. K. H. Morgan-Hughes, J. A.
Citation: J. Holt, I. et al., A New mitochondrial disease associated with mitochondrial DNA heteroplasmy, American journal of human genetics , 46-I(3), 1990, pp. 428-433

Authors: Harding, A. E. Holt, I. J. Sweeney, M. G. Brockington, M. Davis, M. B.
Citation: E. Harding, A. et al., Prenatal diagnosis of mitochondrial DNA8993 T----G disease., American journal of human genetics , 50-I(3), 1992, pp. 629-633

Authors: Collinge, J. Poulter, M. Davis, M. B. Baraitser, M. Owen, F. Crow, T. J. Harding, A. E.
Citation: J. Collinge, et al., Presymptomatic detection or exclusion of prion protein gene defects in families with inherited prion diseases., American journal of human genetics , 49-II(5), 1991, pp. 1351-1354
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