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    De novo c.2455C>T mutation of NPR2 gene in a fetus with shortened long bones and a ventricular septal defect conceived by a mother with a fragile site at 16q22.1 and a father with a rare heterochromatic variant of chromosome 4 from Vietnam

    De novo c.2455C>T mutation of NPR2 gene in a fetus with shortened long bones and a ventricular septal defect conceived by a mother with a fragile site at 16q22.1 and a father with... by Thi Minh Thi Ha, Tran Thao Nguyen Nguyen, Thi Mai Ngan Nguyen, Huu Nguyen Nguyen

    Published 2021-04-01
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