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Public Health Genomics and Precision Health Knowledge Base (v9.0)
PHGKB
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Public Health Genomics Branch
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Precision Health Database|Search|Public Health Genomics and Precision Health Knowledge Base (PHGKB)
Last data update: Apr 25, 2024
. (Total: 63675 Documents since 2012)
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Records 1 - 6 (of 6 Records)
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Disparities[original query]>>Guidelines Related[Product Type]
Guidance on Use of Race, Ethnicity, and Geographic Origin as Proxies for Genetic Ancestry Groups in Biomedical Publications
G Feero et al, JAMA, March 12, 2024
AGA Clinical Practice Update on Risk Stratification for Colorectal Cancer Screening and Post-Polypectomy Surveillance: Expert Review.
Rachel B Issaka et al. Gastroenterology 2023
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Genomic diagnosis and care co-ordination for monogenic inflammatory bowel disease in children and adults: consensus guideline on behalf of the British Society of Gastroenterology and British Society of Paediatric Gastroenterology, Hepatology and Nutrition.
Kammermeier Jochen et al. The lancet. Gastroenterology & hepatology 2023
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[The French Genetic and Cancer Consortium guidelines for multigene panel analysis in hereditary breast and ovarian cancer predisposition].
Moretta Jessica et al. Bulletin du cancer 2018 Sep
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Optimizing use of existing prenatal genetic tests: Screening and diagnostic testing for aneuploidy.
Stoll Katie et al. Seminars in perinatology 2018 Jul
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Future cancer research priorities in the USA: a Lancet Oncology Commission.
Jaffee Elizabeth M et al. The Lancet. Oncology 2017 Nov 18(11) e653-e706
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Page last reviewed:
Feb 1, 2024
Page last updated:
Apr 25, 2024
Content source:
Public Health Genomics Branch in the Division of Blood Disorders and Public Health Genomics
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National Center on Birth Defects and Developmental Disabilities
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