Open AccesseP392: A comprehensive genomic test reporting structure for communicating cancer and incidental findings
Author(s) -
Jordan Sam,
Emma Reble,
Angela Shaw,
Rita Kodida,
Marc Clausen,
Mariana Guitierrez Salazar,
Salma Shickh,
Chloe Mighton,
Christine Elser,
Andrea Eisen,
Seema Panchal,
Carolyn Piccinin,
Melyssa Aronson,
Tracy Graham,
Karen Ott,
Susan Randall Armel,
Kasmintan A. Schrader,
June Carroll,
Iris Cohn,
JoséMario CapoChichi,
Raymond H. Kim,
Jordan LernerEllis,
Yvonne Bombard
Publication year - 2022
Publication title -
genetics in medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.509
H-Index - 128
eISSN - 1530-0366
pISSN - 1098-3600
DOI - 10.1016/j.gim.2022.01.427
Subject(s) - exome sequencing , genomic sequencing , identification (biology) , clinical practice , exome , medicine , test (biology) , health care , patient care , dna sequencing , genome , computational biology , bioinformatics , family medicine , genetics , biology , nursing , mutation , gene , economics , botany , paleontology , economic growth
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