Chromothripsis and ring chromosome 22: a paradigm of genomic complexity in the Phelan-McDermid syndrome (22q13 deletion syndrome) | Journal of Medical Genetics
Phelan-McDermid Syndrome - Child Neurology Foundation
Patients I-V, VII-IX and XI-XIV, who present ring chromosomes 3, 4, 10,... | Download Scientific Diagram
What is Phelan-McDermid syndrome? - Phelan-McDermid Syndrome Foundation
Ring chromosome 15 (a) found in an infant with " ring syndrome "... | Download Scientific Diagram