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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: Apr 29, 2024
. (Total: 6062 publications)
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Year
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Records 1-6 (of 6 Records)
Query Trace:
Hannon WH[original query]
Congenital adrenal hyperplasia cases identified by newborn screening in one- and two-screen states.
Held PK ,
Shapira SK
,
Hinton CF
,
Jones E ,
Hannon WH
,
Ojodu J .
Mol Genet Metab 2015 116 (3) 133-8
Newborn blood spot screening test using multiplexed real-time PCR to simultaneously screen for spinal muscular atrophy and severe combined immunodeficiency.
Taylor JL
,
Lee FK
,
Yazdanpanah GK , Staropoli JF , Liu M , Carulli JP , Sun C , Dobrowolski SF , Hannon WH ,
Vogt RF
.
Clin Chem 2014 61 (2) 412-9
CFTR mutation analysis and haplotype associations in CF patients.
Cordovado SK
,
Hendrix M
,
Greene CN
,
Mochal S
,
Earley MC
,
Farrell PM , Kharrazi M ,
Hannon WH
,
Mueller PW
.
Mol Genet Metab 2012 105 (2) 249-54
Implementation of the first worldwide quality assurance program for cystic fibrosis multiple mutation detection in population-based screening.
Earley MC
,
Laxova A , Farrell PM ,
Driscoll-Dunn R
,
Cordovado S
,
Mogayzel PJ Jr , Konstan MW ,
Hannon WH
.
Clin Chim Acta 2011 412 1376-81
Proficiency testing of human leukocyte antigen-DR and human leukocyte antigen-DQ genetic risk assessment for type 1 diabetes using dried blood spots
Dantonio P
,
Meredith-Molloy N
,
Hagopian WA , She JX , Akolkar B ,
Cordovado SK
,
Hendrix M
,
Henderson LO
,
Hannon WH
,
Vogt RF
.
J Diabetes Sci Technol 2010 4 (4) 929-941
Improving and assuring newborn screening laboratory quality worldwide: 30-year experience at the Centers for Disease Control and Prevention
De Jesus VR
,
Mei JV
,
Bell CJ
,
Hannon WH
.
Semin Perinatol 2010 34 (2) 125-33
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Page last reviewed:
Feb 1, 2024
Page last updated:
Apr 29, 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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