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Updated: Jun 20, 2026

Fluorescent Calcium Imaging and Subsequent In Situ Hybridization for Neuronal Precursor Characterization in Xenopus laevis
Published on: February 18, 2020
Neonatal hypercalcemia due to polymorphisms of the calcium sensing receptor
Michelle M Jack1, Monique L Stone, Roderick Clifton-Bligh
1Department of Endocrinology, Royal North Shore Hospital, St Leonards, NSW, Australia. mmjack@med.usyd.edu.au
Abstract:
Familial hypocalciuric hypercalcemia (FHH) is known to be caused by heterozygous inactivating mutations of the calcium sensing receptor (CaSR) gene. We report an infant with transient neonatal hypercalcemia who was found to be homozygous for a polymorphism at A986S of the CaSR.
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