A RETT SYNDROME CASE WITH NOVEL NON-IDENTICAL MUTATION IN MECP2 GENE. [electronic resource]

By: Contributor(s): Producer: 20160303Description: 387-92 p. digitalISSN:
  • 1015-8146
Subject(s): In: Genetic counseling (Geneva, Switzerland) vol. 26
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Publication Type: Case Reports; Journal Article

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