Autosomal dominant hypocalcaemia caused by a Ca2+-sensing receptor gene mutation

Current protocols in molecular biology

R.K. Dudley · FEBS Letters · 1988 · 6K citations · Full text

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Cloning and characterization of an extracellular Ca2+-sensing receptor from bovine parathyroid

Edward M. Brown, Gerardo Gamba, Daniela Riccardi et al. · Nature · 1993 · 2.6K citations

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Strategies for multilocus linkage analysis in humans.

G.M. Lathrop, J.-M. Lalouel, Cécile Julier et al. · Proceedings of the National Academy of Sciences · 1984 · 2.6K citations · Full text

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A second-generation linkage map of the human genome

Jean Weissenbach, Gàbor Gyapay, Colette Dib et al. · Nature · 1992 · 1.7K citations

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Mutations in the human Ca2+-sensing receptor gene cause familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism

Martin R. Pollak, Edward M. Brown, Yah‐Huei Wu Chou et al. · Cell · 1993 · 1K citations

Genetics, Physiology, Neonatal Severe Hyperparathyroidism +4