Ariana Kariminejad
Kariminejad-Najmabadi Pathology & Genetics Center
91 papers found
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Mutations in Fibronectin Cause a Subtype of Spondylometaphyseal Dysplasia with “Corner Fractures”
Download from europepmc.orgAlx4 relays sequential FGF signaling to induce lacrimal gland morphogenesis
Download from doi.orgTOR1A variants cause a severe arthrogryposis with developmental delay, strabismus and tremor
UploadJuvenile nephronophthisis and dysthyroidism: a rare association
Download from www.ncbi.nlm.nih.govBarber-Say Syndrome and Ablepharon-Macrostomia Syndrome: A Patient's View
Download from www.karger.comMutations in ATP6V1E1 or ATP6V1A Cause Autosomal-Recessive Cutis Laxa
Download from hdl.handle.netPrevalence of common MEFV mutations and carrier frequencies in a large cohort of Iranian populations
Download from doi.orgLethal multiple pterygium syndrome, the extreme end of the RYR1 spectrum
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