ACMG SF v3.1 list for reporting of secondary findings in clinical exome and genome sequencing: A policy statement of the American College of Medical Genetics and Genomics (ACMG)-Reference-Cited by-同舟云学术

ACMG SF v3.1 list for reporting of secondary findings in clinical exome and genome sequencing: A policy statement of the American College of Medical Genetics and Genomics (ACMG)

Published:2022-07 Issue:7 Volume:24 Page:1407-1414
ISSN:1098-3600
Container-title:Genetics in Medicine
language:en
Short-container-title:Genetics in Medicine

Author:

Miller David T.,Lee Kristy,Abul-Husn Noura S.,Amendola Laura M.,Brothers Kyle,Chung Wendy K.,Gollob Michael H.,Gordon Adam S.,Harrison Steven M.,Hershberger Ray E.,Klein Teri E.,Richards Carolyn Sue,Stewart Douglas R.,Martin Christa Lese

Publisher

Elsevier BV

Subject

Genetics (clinical)

Reference21 articles.

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2. Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics;Kalia;Genet Med,2017

3. Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2021 update: a policy statement of the American College of Medical Genetics and Genomics (ACMG);Miller;Genet Med,2021

4. ClinGen Myeloid Malignancy Variant Curation Expert Panel recommendations for germline RUNX1 variants;Luo;Blood Adv,2019

5. The 2016 revision to the World Health Organization classification of myeloid neoplasms and acute leukemia;Arber;Blood,2016

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