Whole-exome-based single nucleotide variants and copy number analysis for prenatal diagnosis of compound heterozygosity of SMPD4

aDepartment of Pediatrics

bDepartment of Ultrasound, Renmin Hospital, Hubei University of Medicine, Shiyan, People's Republic of China

Received 3 February 2024 Accepted 15 April 2024.

*Jun Du and Lin Li contributed equally to this work.

Correspondence to Dinghu Fu, MD, Department of Ultrasound, Renmin Hospital, Hubei University of Medicine, Shiyan, Hubei, People's Republic of China Tel: +86 138 7125 4384; e-mail: [email protected]

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