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Publications by Patrick J Morrison
Mutations in AP2S1 Cause Familial Hypocalciuric Hypercalcemia Type 3
Nature Genetics
Genetics
Familial Urothelial Cell Carcinoma of the Bladder With Autosomal Dominant Inheritance and Late Onset Phenotype
SpringerPlus
Multidisciplinary
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Familial Hypocalciuric Hypercalcemia
Atypical Skeletal Manifestations of Rickets in a Familial Hypocalciuric Hypercalcemia Patient
Bone Research
Endocrinology
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Metabolism
Diabetes
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
Familial Hypocalciuric Hypercalcaemia--Familial Benign Hypercalcaemia: A Review.
Postgraduate Medical Journal
Medicine
ACAN Mutations as a Cause of Familial Short Stature
Clinical Pediatric Endocrinology
Child Health
Endocrinology
Perinatology
Pediatrics
Metabolism
Diabetes
Transcription Factor Mutations as a Cause of Familial Myeloid Neoplasms
Journal of Clinical Investigation
Medicine
Association of Parathyroid Adenoma and Familial Hypocalciuric Hypercalcaemia in a Teenager
European Journal of Endocrinology
Medicine
Endocrinology
Metabolism
Diabetes
Atypical Presentation of Familial Hypocalciuric Hypercalcaemia (FHH1)-would You Recognise It?
Endocrine Abstracts
MUTYH Mutations Do Not Cause HNPCC or Late Onset Familial Colorectal Cancer
Hereditary Cancer in Clinical Practice
Oncology
Genetics