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Public Health Genomics and Precision Health Knowledge Base (v9.0)
PHGKB
About
Public Health Genomics Branch
PHGKB Weekly Horizon Scan
Genomics Precision Health Scan
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COVID-19 GPH (47221)
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State Public Health Genomics Programs Database
State Public Health Genomics Programs Database|Search|PHGKB
Last data update: Dec 23, 2020
. (Total: 319 Documents)
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Disease
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Records 1-11 (of 11 Record(s))
Query Trace:
Informed consent [original query]
The Sudden Death in the Young Case Registry: Collaborating to Understand and Reduce Mortality.
[
Disease
: Sudden Cardiac Death;
Type
: Program;
State
: NA]
Evolution of Hereditary Breast Cancer Genetic Services: Are Changes Reflected in the Knowledge and Clinical Practices of Florida Providers?
[
Disease
: Ovarian Cancer|Breast Cancer;
Type
: Data;
State
: NA]
BRCA1 and BRCA2: Information for Health Care Professionals
[
Disease
: Breast Cancer|Ovarian Cancer;
Type
: Education;
State
: NA]
Hereditary Colon and Rectal Cancer Registry
[
Disease
: Lynch syndrome;
Type
: Data|Program;
State
: NA]
Illinois State Genetics Plan (2007) [PDF 2.04 MB]
[
Disease
: NA;
Type
: General Info;
State
: NA]
BRCA1 & BRCA2
[
Disease
: Breast Cancer|Ovarian Cancer;
Type
: Education;
State
: NA]
Genetic Evaluation and Testing for Hereditary Colorectal Cancer: What You Should Know
[
Disease
: Lynch syndrome;
Type
: Education;
State
: NA]
Cancer Genomics Best Practices for Connecticut Healthcare Providers [PDF 7.80 MB]
[
Disease
: Lynch syndrome|Breast Cancer|Ovarian Cancer;
Type
: Policy|Program;
State
: NA]
Connecticut Department of Public Health Genomics Action Plan [PDF 139 KB]
[
Disease
: NA;
Type
: Policy|Program;
State
: NA]
BRCA 1/2 Surveillance in Michigan, 2008-2012 [PDF 772.97 KB]
[
Disease
: Breast Cancer|Ovarian Cancer;
Type
: Data|Program;
State
: NA]
Enhancing Breast Cancer Genomics Best Practices and Policies in the State of Michigan, 2011-2014
[
Disease
: Breast Cancer|Ovarian Cancer;
Type
: Education|Tools|Program;
State
: NA]
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Page last reviewed:
Feb 1, 2024
Page last updated:
Dec 23, 2020
Content source:
Public Health Genomics Branch in the Division of Blood Disorders and Public Health Genomics
,
National Center on Birth Defects and Developmental Disabilities
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