Article
Identification of ectodysplasin-A receptor gene deletion at 2q12.2 and a potential autosomal MR locus.
European journal of human genetics : EJHG - 1 Jan 2009
Griggs Bradley L, Ladd Sydney, Decker Amy, DuPont Barbara R, Asamoah Alexander, Srivastava Anand K
Abstract excerpt
Mental retardation (MR) is not a common feature observed in patients with classical ectodermal dysplasias (EDs). Several genes responsible for EDs and MR have been identified. However, the causation has yet to be identified in a significant number of patients with either ED or MR. Here, we have molecularly characterized a de novo balanced translocation t(1;6)(p22.1;p22.1) in a female patient who had mild features...
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