Associated Papers
Identification of copy number variants with genome sequencing: Clinical experiences from the NYCKidSeq program.
Bonini KE et al.
Clinical Genetics, 2023
Molecular diagnostic yield of genome sequencing versus targeted gene panel testing in racially and ethnically diverse pediatric patients.
Abul-Husn NS et al.
Medrxiv : the Preprint Server for Health Sciences, 2023
36993157 (PubMed )
Supplement: media-2.xlsx › eTable_5
Analyzing Genetic Differences Between Sporadic Primary and Secondary/Tertiary Hyperparathyroidism by Targeted Next-Generation Panel Sequencing.
Hong YA et al.
Endocrine Pathology, 2021
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