Search Results - Kolsoum InanlooRahatloo
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Intellectual disability associated with craniofacial dysmorphism due to POLR3B mutation and defect in spliceosomal machinery by Mostafa Saghi, Kolsoum InanlooRahatloo, Afagh Alavi, Kimia Kahrizi, Hossein Najmabadi
Published 2022Call Number: Loading…Connect to this object online.
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