Cuneo, B F Evolution of latent hypoparathyroidism in familial 22q11 deletion syndrome. [electronic resource] - American journal of medical genetics Mar 1997 - 50-5 p. digital Publication Type: Case Reports; Journal Article; Research Support, U.S. Gov't, P.H.S. ISSN: 0148-7299 Subjects--Topical Terms: AdolescentAdultAgedChild, PreschoolChromosome DeletionChromosomes, Human, Pair 22Evolution, MolecularFemaleHumansHypoparathyroidism--geneticsMalePedigreeSyndrome