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Public Health Genomics and Precision Health Knowledge Base (v9.0)
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CDC-Authored Genomics and Precision Health Publications Database|Home|Public Health Genomics and Precision Health Knowledge Base (PHGKB)
CDC-Authored Genomics and Precision Health Publications Database
Last data update: Mar 25, 2024
. (Total: 5510 publications)
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Records 1-6 (of 6 Records)
Query Trace:
all>>Rodolfo Valdez[CDC Author]
Preventive care services and health behaviors in children with fragile X syndrome.
Gilbertson KE
,
Jackson HL
,
Dziuban EJ
,
Sherman SL , Berry-Kravis EM , Erickson CA ,
Valdez R
.
Disabil Health J 2019 12 (4) 564-573
PhenX measures for phenotyping rare genetic conditions.
Phillips M , Grant T , Giampietro P , Bodurtha J ,
Valdez R
,
Maiese DR , Hendershot T , Terry SF , Hamilton CM .
Genet Med 2017 19 (7) 834-837
The need for a next-generation public health response to rare diseases.
Valdez R
,
Grosse SD
,
Khoury MJ
.
Genet Med 2016 19 (5) 489-490
Public Health and Rare Diseases: Oxymoron No More.
Valdez R
,
Ouyang L
,
Bolen J
.
Prev Chronic Dis 2016 13 E05
Health beliefs among individuals at increased familial risk for type 2 diabetes: implications for prevention.
Dorman JS ,
Valdez R
,
Liu T
,
Wang C , Rubinstein WS , O'Neill SM , Acheson LS , Ruffin MT4th ,
Khoury MJ
.
Diabetes Res Clin Pract 2012 96 (2) 156-62
Influence of familial risk on diabetes risk-reducing behaviors among U.S. adults without diabetes.
Chang MH
,
Valdez R
,
Ned RM
,
Liu T
,
Yang Q
,
Yesupriya A
,
Dowling NF
,
Meigs JB ,
Bowen MS
,
Khoury MJ
.
Diabetes Care 2011 34 (11) 2393-9
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Page last reviewed:
Feb 1, 2024
Page last updated:
Mar 25, 2024
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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