Associated Papers
Prenatal genetic diagnosis associated with fetal ventricular septal defect: an assessment based on chromosomal microarray analysis and exome sequencing.
Wang Y et al.
Frontiers in Genetics, 2023
Heterozygous Recurrent Mutations Inducing Dysfunction of ROR2 Gene in Patients With Short Stature.
Gui B et al.
Frontiers in Cell and Developmental Biology, 2021
Targeted next-generation sequencing-based molecular diagnosis of congenital hand malformations in Chinese population.
Qin L et al.
Scientific Reports, 2018
30143665 (PubMed )
Supplement: 41598_2018_30940_MOESM1_ESM.pdf
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