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BACINO, CARLOS
One or more keywords matched the following items that are connected to
BACINO, CARLOS
Item Type
Name
Academic Article
WDR35 mutation in siblings with Sensenbrenner syndrome: a ciliopathy with variable phenotype.
Academic Article
Craniofacial and anthropometric phenotype in ankyloblepharon-ectodermal defects-cleft lip/palate syndrome (Hay-Wells syndrome) in a cohort of 17 patients.
Concept
Ectodermal Dysplasia
Academic Article
UBR7 functions with UBR5 in the Notch signaling pathway and is involved in a neurodevelopmental syndrome with epilepsy, ptosis, and hypothyroidism.
Search Criteria
Ectodermal Dysplasia