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Publications by G. Vezzoli
A Novel Germline Inactivating Mutation in the CASR Gene in an Italian Kindred Affected by Familial Hypocalciuric Hypercalcemia
European Journal of Endocrinology
Medicine
Endocrinology
Metabolism
Diabetes
Related publications
Familial Hypocalciuric Hypercalcemia
Mutations in AP2S1 Cause Familial Hypocalciuric Hypercalcemia Type 3
Nature Genetics
Genetics
Atypical Skeletal Manifestations of Rickets in a Familial Hypocalciuric Hypercalcemia Patient
Bone Research
Endocrinology
Physiology
Histology
Metabolism
Diabetes
A Novel Pathogenic Germline Mutation in the Adenomatous Polyposis Coli Gene in a Chinese Family With Familial Adenomatous Coli
Oncotarget
Oncology
Novel Mutation in the AAAS Gene in a Severely Affected Triple-A Syndrome Patient
Endocrinology & Metabolic Syndrome
Familial Hypocalciuric Hypercalcaemia--Familial Benign Hypercalcaemia: A Review.
Postgraduate Medical Journal
Medicine
Confirmation of the HOXB13 G84E Germline Mutation in Familial Prostate Cancer
Cancer Epidemiology Biomarkers and Prevention
Medicine
Epidemiology
Oncology
A Novel Missense Mutation in the CYLD Gene in a Spanish Family With Multiple Familial Trichoepithelioma
Archives of Dermatology
GP56 Severe Hypercalcemic Crisis in an Infant With Idiopathic Infantile Hypercalcemia Caused by Mutation in CYP24A1 Gene
