Skip to Main Content

Paper Details

Preconception Carrier Screening by Genome Sequencing: Results from the Clinical Laboratory.
Am J Hum Genet
28
2018
F8, RNA, copy, genes, hemophilia A, hemorrhage, hereditary hemochromatosis, missense variants, non-coding regions, participants, splice-site variants, women
Author NameAffiliation
Yassmine AkkariOregon Health & Science University
Allison L CreasonOregon Health & Science University
Michael O DorschnerUniversity of Washington
Michael O DorschnerUniversity of Washington
Deborah A NickersonUniversity of Washington
Deborah A NickersonUniversity of Washington
Gail P JarvikUniversity of Washington
Gail P JarvikUniversity of Washington
Laura M AmendolaUniversity of Washington
Tia L KauffmanCenter for Health Research, Kaiser Permanente Northwest
Benjamin S WilfondUniversity of Washington, USA Treuman Katz Center for Pediatric Bioethics, Seattle Children's Hospital
Katrina A B GoddardCenter for Health Research, Kaiser Permanente Northwest
Carolyn Sue RichardsOregon Health & Science University
  • 1 - 13

Datasets

Release 1.2