Associated Papers
Exome sequencing in every pregnancy? Results of trio exome sequencing in structurally normal fetuses.
Levy M et al.
Prenatal Diagnosis, 2025
The Challenges of Performing Exome Sequencing in Structurally Normal Fetuses.
Chandler N et al.
Prenatal Diagnosis, 2025
Insights into the ANKRD11 variants and short-stature phenotype through literature review and ClinVar database search.
He D et al.
Orphanet Journal of Rare Diseases, 2024
39135054 (PubMed )
Supplement: 13023_2024_3301_MOESM1_ESM.xlsx › Sheet1
Diagnostic yield after next-generation sequencing in pediatric cardiovascular disease.
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Hgg Advances, 2024
38521975 (PubMed )
Supplement: mmc2.xlsx › Supplementary_table_2
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