Search

Subject Deafness -- Genetics -- Screening

1. A protocol for whole-exome sequencing in newborns with congenital deafness: a prospective population-based cohort. Issue 1 (14th September 2017)

Authors:
Downie, Lilian; Halliday, Jane L; Burt, Rachel A; Lunke, Sebastian; Lynch, Elly; Martyn, Melissa; Poulakis, Zeffie; Gaff, Clara; Sung, Valerie; Wake, Melissa; Hunter, Matthew; Saunders, Kerryn; Rose, Elizabeth; Rehm, Heidi L; Amor, David J
Journal:
BMJ paediatrics open
Issue:
Volume 1:Issue 1(2017)
Page Start:
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

Limit your search