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craniofacial and skeletal problems

From The Labs

Mutations in CWC27 result in spectrum of conditions

April 13, 2017 blindness, craniofacial and skeletal problems, CWC27, Genetics, Retinitis pigmentosa, spliceosome, whole exome sequencing

Mingchu Xu searches for genes linked to retinitis pigmentosa, a condition of the retina characterized by progressive development of night blindness and tunnel vision, sometimes from

From the Labs Image of the Month:

From the Labs: Human retinal organoid.