Risk factors for primary congenital glaucoma in the National Birth Defects Prevention Study

Author:

Forestieri Nina E.1ORCID,Desrosiers Tania A.2,Freedman Sharon F.3,Aylsworth Arthur S.4,Voltzke Kristin2,Olshan Andrew F.2,Meyer Robert E.15,

Affiliation:

1. North Carolina Birth Defects Monitoring Program, State Center for Health Statistics Raleigh North Carolina

2. Department of EpidemiologyGillings School of Global Public Health, University of North Carolina at Chapel Hill Chapel Hill North Carolina

3. Department of Ophthalmology and PediatricsDuke University Medical Center Durham North Carolina

4. Department of Pediatrics and GeneticsUniversity of North Carolina at Chapel Hill Chapel Hill North Carolina

5. Department of Maternal and Child HealthGillings School of Global Public Health, University of North Carolina at Chapel Hill Chapel Hill North Carolina

Funder

University of North Carolina at Chapel Hill

Centers for Disease Control and Prevention

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference41 articles.

1. Screening of CYP1B1 and LTBP2 genes in Saudi families with primary congenital glaucoma: Genotype‐phenotype correlation;Abu‐Amero K. K.;Molecular Vision,2011

2. Null mutations in LTBP2 cause primary congenital glaucoma;Ali M.;American Journal of Human Genetics,2009

3. Angiotensin‐converting enzyme inhibitors and the risk of congenital malformations;Bateman B. T.;Obstetrics and Gynecology,2017

4. Maternal treatment with opioid analgesics and risk for birth defects;Broussard C. S.;American Journal of Obstetrics and Gynecology,2011

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