Phelan McDermid: Difference between revisions

Revision as of 18:49, 24 September 2018

(PMS^[1]) is a rare genetic condition caused by deletion of terminal end of chromosome 22^[2] , about 44% of people develops seizures^[3]

↑ https://www.ncbi.nlm.nih.gov/books/NBK1198/
↑ Phelan McDermid The 22q13,3 deletion syndrome or Phelan McDermid syndrome Mol.syndromology
↑ DMSF

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			[[nl:Syndroom van Phelan-McDermid]]