Molecular screening of In2G (c.293-13A/C>G) mutation and detected genotypes among the Macedonian patients with classical form of 21-hydroxylase deficiency

Journal
International Journal of Neonatal Screening
Date Issued
2018-10-14
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11th ISNS - Bratislava, 2018, P26.pdf

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1.14 MB

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Adobe PDF

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(MD5):4aa0ba6122a25670033892a68b13dcd5