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Browsing by Author Slyper, A. H.

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Autosomal dominant pseudohypoparathyroidism type Ib is associated with a heterozygous microdeletion that likely disrupts a putative imprinting control element of GNASBastepe, M.; Frohlich, L. F.; Hendy, G. N.; Indridason, O. S.; Josse, R. G.; Koshiyama, H.; Korkko, J.; Nakamoto, J. M.; Rosenbloom, A. L.; Slyper, A. H.; Sugimoto, T.; Tsatsoulis, A.; Crawford, J. D.; Juppner, H.24-Nov-2015-
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