Pages that link to "Q38248966"

The following pages link to GNAS mutations in Pseudohypoparathyroidism type 1a and related disorders (Q38248966):

Displaying 32 items.

• Epidemiology and Diagnosis of Hypoparathyroidism (Q33570602) (← links)
• Rare Variant Analysis of Human and Rodent Obesity Genes in Individuals with Severe Childhood Obesity (Q33854345) (← links)
• Pseudohypoparathyroidism: one gene, several syndromes (Q34547669) (← links)
• Progressive osseous heteroplasia: diagnosis, treatment, and prognosis (Q35063732) (← links)
• Resting Energy Expenditure Is Decreased in Pseudohypoparathyroidism Type 1A. (Q36716035) (← links)
• Epidemiology and Health-Related Quality of Life in Hypoparathyroidism in Norway (Q37147509) (← links)
• A Novel T55A Variant of Gs α Associated with Impaired cAMP Production, Bone Fragility, and Osteolysis (Q37192455) (← links)
• Pseudohypoparathyroidism and Gsα-cAMP-linked disorders: current view and open issues. (Q38816341) (← links)
• Genetics of Short Stature (Q39286284) (← links)
• Pseudohypoparathyroidism type 1a due to a novel mutation in the GNAS gene (Q42413924) (← links)
• Ossifications in Albright Hereditary Osteodystrophy: Role of Genotype, Inheritance, Sex, Age, Hormonal Status, and BMI. (Q47236686) (← links)
• Clinical and genetic characteristics of Pseudohypoparathyroidism in the Chinese population. (Q47599083) (← links)
• The GNASR201C mutation associated with clonal hematopoiesis supports transplantable hematopoietic stem cell activity (Q47633846) (← links)
• A novel deletion involving GNAS exon 1 causes PHP1A and further refines the region required for normal methylation at exon A/B. (Q47697488) (← links)
• Obstructive Sleep Apnea and Otolaryngologic Manifestations in Children with Pseudohypoparathyroidism (Q49893228) (← links)
• Hypoparathyroidism. (Q51799713) (← links)
• Disease-Causing Mutations in the G Protein Gαs Subvert the Roles of GDP and GTP. (Q52600114) (← links)
• Constitutive stimulatory G protein activity in limb mesenchyme impairs bone growth. (Q52730955) (← links)
• Cognitive and behavioral phenotype of children with pseudohypoparathyroidism type 1A. (Q53495546) (← links)
• (Epi)genotype-Phenotype Analysis in 69 Japanese Patients With Pseudohypoparathyroidism Type I. (Q53709803) (← links)
• Identification of a Novel Mutation in a Family with Pseudohypoparathyroidism Type 1a. (Q54961774) (← links)
• Genetic Approaches to Metabolic Bone Diseases (Q57790364) (← links)
• Case report: An infantile lethal form of Albright hereditary osteodystrophy due to a mutation (Q57823862) (← links)
• Pseudohypoparathyroidism (Q58547778) (← links)
• A case of pseudohypoparathyroidism type Ia with a novel frameshift mutation in the gene: early diagnosis of osteoma cutis by skin biopsy (Q61804936) (← links)
• Diagnosis and management of pseudohypoparathyroidism and related disorders: first international Consensus Statement (Q63443793) (← links)
• Unusual case of hypocalcaemia (Q89000386) (← links)
• Cutaneous nodules and a novel GNAS mutation in a Chinese boy with pseudohypoparathyroidism type Ia: A case report and review of literature (Q89942807) (← links)
• Identification of a novel GNAS mutation in a case of pseudohypoparathyroidism type 1A with normocalcemia (Q90641522) (← links)
• Central precocious puberty in a boy with pseudohypoparathyroidism type Ia due to a novel GNAS mutation (Q92097307) (← links)
• Management of pseudohypoparathyroidism (Q92399677) (← links)
• Hypoparathyroidism, deafness and renal dysplasia (HDR) syndrome: 20 years after the identification of the first GATA3 mutations (Q95650215) (← links)