Donnice Michel

HERV‐mediated genomic rearrangement of EYA1 in an individual with branchio‐oto‐renal syndrome

P. Stankiewicz, Z. Xia, S. Cheung, 2010, American journal of medical genetics. Part A.

A pathogenic UFSP2 variant in an autosomal recessive form of pediatric neurodevelopmental anomalies and epilepsy

N. Grishin, R. Deberardinis, J. Pei, 2021, Genetics in Medicine.

Clinical Exome Studies Have Inconsistent Coverage.

Jason Y. Park, A. Scheuerle, J. Kozlitina, 2020, Clinical chemistry.