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PedAM

Pediatric Disease Annotations & Medicines




Disease dwarfism
Phenotype C0007766|cranial aneurysm
Sentences 1
PubMedID- 26231886 Identification of two novel critical mutations in pcnt gene resulting in microcephalic osteodysplastic primordial dwarfism type ii associated with multiple intracranial aneurysms.

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