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craniofacial and skeletal problems

From The Labs

Mutations in CWC27 result in spectrum of conditions

April 13, 2017 Ana Rodríguez 0 Comments 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 features a cluster of metastatic cancer cells found in the blood of mice with breast cancer tumors. Image courtesy of the Dr. Xiang Zhang lab.

Tips to Prepare for Hurricane Season

Baylor College of Medicine experts share advice on how to stay prepared throughout hurricane season.