Associated Papers
Use of genome sequencing to hunt for cryptic second-hit variants: analysis of 31 cases recruited to the 100 000 Genomes Project.
Moore AR et al.
Journal of Medical Genetics, 2023
37558402 (PubMed )
Supplement: jmg-2023-109362supp001.pdf
Novel Glial Cells Missing-2 (GCM2) variants in parathyroid disorders.
Canaff L et al.
European Journal of Endocrinology, 2022
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