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Publications by Minh H. Ta
Novel Variants of CYP21A2 in Vietnamese Patients With Congenital Adrenal Hyperplasia
Molecular genetics & genomic medicine
Genetics
Molecular Biology
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Functional Studies of Novel CYP21A2 Mutations Detected in Norwegian Patients With Congenital Adrenal Hyperplasia
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Four Clinical Variants of Congenital Adrenal Hyperplasia
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Complement Component 4 Copy Number Variation and CYP21A2 Genotype Associations in Patients With Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
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Current Opinion in Endocrinology, Diabetes and Obesity
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Letter: Congenital Adrenal Hyperplasia.
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Parental Management of Adrenal Crisis in Children With Congenital Adrenal Hyperplasia
Journal for specialists in pediatric nursing : JSPN
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Bone Mineral Status in Children With Congenital Adrenal Hyperplasia
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Testicular Nodules in Congenital Adrenal Hyperplasia (Cah)
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