Myoclonic movement disorder associated with microdeletion of chromosome The 22Q11.2 Deletion Syndrome As a Model for Idiopathic Scoliosis DocsLib Systematic assessment of atypical deletions reveals genotypephenotype Sindrome de Duplicacin 22q11 2 Nicole Gorena uDocz Hypoparathyroidism MedLink Neurology DiGeorge (22q11.2 Deletion) Syndrome PsychDB
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