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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.
Ha TMT, Nguyen TTN, Nguyen TMN, Nguyen HN. Ha TMT, et al. Among authors: nguyen tmn, nguyen hn, nguyen ttn. Mol Genet Genomic Med. 2021 Apr;9(4):e1637. doi: 10.1002/mgg3.1637. Epub 2021 Mar 13. Mol Genet Genomic Med. 2021. PMID: 33713577 Free PMC article.
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