Whole-exome sequencing identifies de novo mutation in the COL1A1 gene to underlie the severe osteogenesis imperfecta

Exome sequencing identifies de novo mutation underlying severe osteogenesis imperfecta - new in Human #Genomics http://t.co/LWNUGHbYGN

Whole-exome sequencing identifies de novo mutation in the COL1A1 gene to underlie the severe osteogenesis… http://t.co/1aNii74qLW

Whole-exome sequencing identifies de novo mutation in the COL1A1 gene to underlie the severe osteogenesis imperfecta http://t.co/b9jMa9AdBu

Whole-exome sequencing identifies de novo mutation in the COL1A1 gene to underlie the severe osteogenesis imperfecta http://t.co/b9jMa9AdBu