Novel homozygous nonsense mutation associated with Bardet–Biedl syndrome in fetuses with congenital renal malformation
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
General Medicine
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3. Delineating the Spectrum of Genetic Variants Associated with Bardet-Biedl Syndrome in Consanguineous Pakistani Pedigrees;Genes;2023-02-03
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