Associated Papers
Novel variants of NEK9 associated with neonatal arthrogryposis: Two case reports and a literature review.
Liu F et al.
Frontiers in Genetics, 2022
Rapid whole exome sequencing in pregnancies to identify the underlying genetic cause in fetuses with congenital anomalies detected by ultrasound imaging.
Deden C et al.
Prenatal Diagnosis, 2020
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