pseudohypoparathyroidism type Ia

pseu·do·hy·po·par·a·thy·roid·ism type Ia

pseudohypoparathyroidism believed to be due to a defect in the G protein associated with adenylate cyclase (probably autosomal dominant).
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Pseudohypoparathyroidism type Ia from maternal but not paternal transmission of a Gsalpha gene mutation.
Infantile hypothyroidism in two sibs: an unusual presentation of pseudohypoparathyroidism type Ia. J Pediatr 1985;107:919-22.
Growth hormone-releasing hormone resistance in pseudohypoparathyroidism type Ia: new evidence for imprinting of the Gs-alpha gene.
Cognitive impairment is prevalent in pseudohypoparathyroidism type Ia, but not in pseudopseudohypoparathyroidism: possible cerebral imprinting of Gsalpha.
A family of pseudohypoparathyroidism type Ia with an 850-kb submicroscopic deletion encompassing the whole GNAS locus.
Hypothyroidism in patients with pseudohypoparathyroidism type Ia: clinical evidence of resistance to TSH and TRH.
Pseudohypoparathyroidism type Ia. Albright hereditary osteodystrophy: a model for research on G protein-coupled receptors and genomic imprinting.
Pseudohypoparathyroidism type Ia (PHP-Ia) is characterized by multihormone resistance and Albright hereditary osteodystrophy.
Brachydactyly in 14 genetically characterized pseudohypoparathyroidism type Ia patients.
Growth hormone releasing hormone resistance in pseudohypoparathyroidism type ia: new evidence for imprinting of the Gs a gene.
Pseudohypoparathyroidism type Ia and pseudo-pseudohypoparathyroidism: the growing spectrum of GNAS inactivating mutations.
Early manifestation of calcinosis cutis in pseudohypoparathyroidism type Ia associated with a novel mutation in the GNAS gene.
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