Co-Authors
This is a "connection" page, showing publications co-authored by HONGZHENG DAI and LIESBETH VOSSAERT.
Connection Strength
0.118
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MED12 Loss-of-Function Variants as a Cause of Congenital Diaphragmatic Hernia in Females With Hardikar Syndrome and Nonspecific Intellectual Disability. Am J Med Genet A. 2024 Aug 30; e63868.
Score: 0.062
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Evaluation of an automated genome interpretation model for rare disease routinely used in a clinical genetic laboratory. Genet Med. 2023 06; 25(6):100830.
Score: 0.056