Millichap, J. G. (2000). MECP2 Mutations and Rett Syndrome Phenotypes. Pediatric Neurology Briefs Publishers.
Dyfyniad Arddull ChicagoMillichap, J Gordon. MECP2 Mutations and Rett Syndrome Phenotypes. Pediatric Neurology Briefs Publishers, 2000.
Dyfyniad MLAMillichap, J Gordon. MECP2 Mutations and Rett Syndrome Phenotypes. Pediatric Neurology Briefs Publishers, 2000.
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