Thyroid gland and carotid artery anomalies in 22q11.2 deletion syndromes
Author:
Publisher
Wiley
Subject
Otorhinolaryngology
Reference27 articles.
1. Prevalence of 22q11 microdeletion;Tezenas;J Med Genet,1996
2. Prevalence of 22q11 microdeletions in DiGeorge and velocardiofacial syndromes: implications for genetic counselling and prenatal diagnosis;Driscoll;J Med Genet,1993
3. Defining the clinical spectrum of deletion 22q11.2;Robin;J Pediatr,2005
4. Velocardiofacial syndrome;Shprintzen;Otolaryngol Clin North Am,2000
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1. Endocrine manifestations in adults with 22q11.2 deletion syndrome: a retrospective single-center cohort study;Journal of Endocrinological Investigation;2024-02-03
2. Risk of thyroid neoplasms in patients with 22q11.2 deletion and DiGeorge-like syndromes: an insight for follow-up;Frontiers in Endocrinology;2023-08-10
3. Characterization of Autoimmune Thyroid Disease in a Cohort of 73 Paediatric Patients Affected by 22q11.2 Deletion Syndrome: Longitudinal Single-Centre Study;Genes;2022-08-28
4. Hashimoto’s Thyroiditis and Graves’ Disease in Genetic Syndromes in Pediatric Age;Genes;2021-02-04
5. Disorders of the Thyroid in the Newborn and Infant;Sperling Pediatric Endocrinology;2021
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