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Public Health Genomics and Precision Health Knowledge Base (v10.0)
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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: Dec 02, 2024
. (Total: 6432 publications)
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Records 1-4 (of 4 Records)
Query Trace:
Cragan JD[original query]
Prevalence and descriptive epidemiology of Turner syndrome in the United States, 2000-2017: A report from the National Birth Defects Prevention Network.
Martin-Giacalone BA , Lin AE , Rasmussen SA , Kirby RS , Nestoridi E , Liberman RF , Agopian AJ , Carey JC ,
Cragan JD
,
Forestieri N , Leedom V , Boyce A , Nembhard WN , Piccardi M , Sandidge T , Shan X , Shumate CJ ,
Stallings EB
,
Stevenson R , Lupo PJ .
Am J Med Genet A 2023 191 (5) 1339-1349
Frequency of prenatal cytogenetic diagnosis and pregnancy outcomes by maternal race-ethnicity, and the effect on the prevalence of trisomy 21, Metropolitan Atlanta, 1996-2005.
Jackson JM
,
Crider KS
,
Cragan JD
,
Rasmussen SA
,
Olney RS
.
Am J Med Genet A 2014 164 (1) 70-6
Trends in cytogenetic testing and identification of chromosomal abnormalities among pregnancies and children with birth defects, metropolitan Atlanta, 1968-2005.
Jackson JM
,
Crider KS
,
Rasmussen SA
,
Cragan JD
,
Olney RS
.
Am J Med Genet A 2011 158A (1) 116-23
The contribution of chromosomal abnormalities to congenital heart defects: a population-based study.
Hartman RJ
,
Rasmussen SA
,
Botto LD ,
Riehle-Colarusso T
,
Martin CL ,
Cragan JD
,
Shin M
,
Correa A
.
Pediatr Cardiol 2011 32 (8) 1147-57
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Page last reviewed:
Feb 1, 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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