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Journal of Medical Genetics|March 15, 2020
Cancer Variant Interpretation Group UK (CanVIG-UK): an exemplar national subspecialty multidisciplinary networkAlice Garrett, Alison Callaway, Miranda Durkie, et al.
Surgery|June 29, 2021
Multiple endocrine neoplasia type 1 in children and adolescents: Clinical features and treatment outcomesOmair A Shariq, Kate E Lines, Katherine A English, et al.
Diagnostic Molecular Pathology : the American Journal of Surgical Pathology, Part B|November 7, 2013
A comparison of methods for EGFR mutation testing in non-small cell lung cancerElizabeth C Young, Martina M Owens, Idowu Adebiyi, et al.
Human Molecular Genetics|March 17, 2012
Identification of 70 calcium-sensing receptor mutations in hyper- and hypo-calcaemic patients: evidence for clustering of extracellular domain mutations at calcium-binding sitesFadil M Hannan, M Andrew Nesbit, Chen Zhang, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 22, 2023
Secondary (additional) findings from the 100,000 Genomes Project: Disease manifestation, health care outcomes, and costs of disclosureJoshua Nolan, James Buchanan, John Taylor, et al.
Human Molecular Genetics|June 18, 2015
Adaptor protein-2 sigma subunit mutations causing familial hypocalciuric hypercalcaemia type 3 (FHH3) demonstrate genotype-phenotype correlations, codon bias and dominant-negative effectsFadil M Hannan, Sarah A Howles, Angela Rogers, et al.
The Journal of Clinical Endocrinology and Metabolism|December 16, 2014
Heterogeneous genetic background of the association of pheochromocytoma/paraganglioma and pituitary adenoma: results from a large patient cohortJudit Dénes, Francesca Swords, Eleanor Rattenberry, et al.
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