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.
Zonana J, Gault J, Davies KJ, Jones M, Browne D, Litt M, Brockdorff N, Rastan S, Clarke A, Thomas NS. Am J Hum Genet. 1993 Jan; 52(1):78-84.