A Case of CATCH22 Syndrome with Normal Parathyroid Function
Author:
Affiliation:
1. Department of Endocrinology and Metabolism, Ajou University School of Medicine, Suwon, Korea.
2. Department of Medical Genetics, Ajou University School of Medicine, Suwon, Korea.
Publisher
Korean Endocrine Society
Subject
Endocrinology,Endocrinology, Diabetes and Metabolism
Link
https://synapse.koreamed.org/pdf/10.3803/EnM.2012.27.2.151
Reference14 articles.
1. Noonan's and DiGeorge syndromes with monosomy 22q11.
2. Defining the Clinical Spectrum of Deletion 22q11.2
3. Prevalence of 22q11 microdeletions in DiGeorge and velocardiofacial syndromes: implications for genetic counselling and prenatal diagnosis.
4. Velocardiofacial syndrome, DiGeorge syndrome: the chromosome 22q11.2 deletion syndromes
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