← Evidence map

ArticleMolecular genetics & genomic medicine2021

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.

Thi Minh Thi Ha et al.PubMed ↗Full text ↗Publisher ↗

No numbers read from the abstract.

Not cited yet

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. | OpenQuestion