Clinical features and tubulin folding cofactor E gene analysis in Iranian patients with Sanjad–Sakati syndrome
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology, and Child Health
Reference22 articles.
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2. Partial agenesis of corpus callosum in Sanjad–Sakati syndrome (p-ACC);Alghasab;Can J Neurol Sci,2012
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2. Hypoparathyroidism-retardation-dysmorphism syndrome—Clinical insights from a large longitudinal cohort in a single medical center;Frontiers in Pediatrics;2022-07-22
3. Homozygous TBCE Gene Mutation c.155-166del in a Libyan Patient with Sanjad-Sakati Syndrome: Same Gene Mutation Responsible in All Arab Ethnic Patients;Journal of Pediatric Genetics;2022-06-15
4. Oral Facial Manifestations of Sanjad–Sakati Syndrome: A Literature Review;Children;2022-03-22
5. Overlapping phenotype comprising Kenny‐Caffey type 2 and Sanjad‐Sakati syndromes: The first case report;American Journal of Medical Genetics Part A;2020-10-03
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