Detection of a molecular deletion at the DXS732 locus in a patient with X-linked hypohidrotic ectodermal dysplasia (EDA), with the identification of a unique junctional fragment

J. Zonana, J. Gault, K. J.P. Davies, M. Jones, D. Browne, M. Litt, N. Brockdorff, S. Rastan, A. Clarke, N. S.T. Thomas

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