Disease: Hypoparathyroidism-retardation-dysmorphism syndrome
- A case of severe TBCE-negative hypoparathyroidism-retardation-dysmorphism syndrome: Case report and literature review
- Additional Tunisian patients with Sanjad-Sakati syndrome: A review toward a consensus on diagnostic criteria
- Clinical features and tubulin folding cofactor E gene analysis in Iranian patients with Sanjad-Sakati syndrome
- Congenital neuroblastoma in a neonate with hypoparathyroidism-retardation-dysmorphism syndrome
- Corneal opacification in Sanjad-Sakati syndrome
- Endocrinological Manifestations of Sanjad-Sakati Syndrome
- Expanding the Phenotypic Spectrum of Kenny-Caffey Syndrome
- Homozygous <em>TBCE</em> Gene Mutation c.155-166del in a Libyan Patient with Sanjad-Sakati Syndrome: Same Gene Mutation Responsible in All Arab Ethnic Patients
- Hypoparathyroidism in children: a study of eight cases
- Hypoparathyroidism-Retardation-Dysmorphism Syndrome due to a Variant in the Tubulin-Specific Chaperone E Gene as a Cause of Combined Immune Deficiency
- Hypoparathyroidism-retardation-dysmorphism syndrome-Clinical insights from a large longitudinal cohort in a single medical center
- Kenny-Caffey syndrome and its related syndromes
- Measurement of the Neutrophils Count and Oxidative Burst in Neutrophils of Patients with Sanjad Sakati Syndrome
- Multiple Endocrine Deficiencies are Common in Hypoparathyroidism-Retardation-Dysmorphism Syndrome
- Overlapping phenotype comprising Kenny-Caffey type 2 and Sanjad-Sakati syndromes: The first case report
- Sanjad Sakati syndrome and sleep-disordered breathing: an undisclosed association
- Sanjad-Sakati syndrome with macrocytic anemia and failure to thrive: a case from South Jordan
- Sanjad-Sakati Syndrome: Oral Health Care