Multilocus disease-causing genomic variations for Mendelian disorders: role of systematic phenotyping and implications on genetic counselling
暂无分享，去创建一个
K. Girisha | A. Shukla | S. Nampoothiri | Y. Ramesh Bhat | Michelle C do Rosario | P. Kaur | Suvasini Sharma | S. Bielas | P. Majethia | D. Narayanan | Divya Udyawar | Narayanaswamy Suresh | Puneeth H. Somashekar | Lakshmi Priya Rao | Neethukrishna Kausthubham | Shruti R. Pande | A. Shrikiran | Shruti Pande | Michelle C. do Rosario