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Ophthalmic Genetics Volume 36, 2015 - Issue 1
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Letter to the Journal

A Case of 22q11.2 Deletion Syndrome with Peters Anomaly, Congenital Glaucoma, and Heterozygous Mutation in CYP1B1

Linda M. ReisDepartment of Pediatrics and Children’s Research Institute at the Medical College of Wisconsin and Children’s Hospital of Wisconsin, Milwaukee, WI, USA,
,
Rebecca C. TylerDepartment of Pediatrics and Children’s Research Institute at the Medical College of Wisconsin and Children’s Hospital of Wisconsin, Milwaukee, WI, USA,
,
Roberto ZoriDivision of Genetics and Metabolism, University of Florida, Gainesville, FL, USA, and
,
Jennifer BurgessDivision of Genetics and Metabolism, University of Florida, Gainesville, FL, USA, and
,
Jennifer MuellerDivision of Genetics and Metabolism, University of Florida, Gainesville, FL, USA, and
&
Elena V. SeminaDepartment of Pediatrics and Children’s Research Institute at the Medical College of Wisconsin and Children’s Hospital of Wisconsin, Milwaukee, WI, USA, ;Department of Cell Biology, Neurobiology and Anatomy at the Medical College of Wisconsin, Milwaukee, WI, USACorrespondence[email protected]
Pages 92-94 | Received 06 Aug 2013, Accepted 07 Aug 2013, Published online: 11 Sep 2013

References

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