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Publications by Nazli B. McDonnell
Complement Component 4 Copy Number Variation and CYP21A2 Genotype Associations in Patients With Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
Human Genetics
Genetics
The Phenotypic Spectrum of Contiguous Deletion ofCYP21A2and Tenascin XB: Quadricuspid Aortic Valve and Other Midline Defects
American Journal of Medical Genetics, Part A
Genetics
