Last Posted: Jan 15, 2019
- Autosomal recessive protein C deficiency
From NCATS - Congenital analbuminemia
From NCATS - Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation
From NCATS - Deafness-lymphedema-leukemia syndrome
From NCATS - Diffuse intrinsic pontine glioma
From NCATS - Dissociative seizures
From NCATS - Epidermoid brain cyst
From NCATS - Episodic angioedema with eosinophilia
From NCATS - Genuine diffuse phlebectasia
From NCATS - Giant cell tumor of bone
From NCATS
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