Seven new cases of cayler cardiofacial syndrome with chromosome 22q11.2 deletion, including a familial case
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference8 articles.
1. Cardiofacial syndrome. Congenital heart disease and facial weakness, a hitherto unrecognized association.
2. Cayler cardiofacial syndrome and del22qll: Part of the CATCH22 phenotype
3. Familial Asymmetric Crying Facies
4. Congenital hypoplasia of depressor anguli oris muscle: A genetically determined condition?
5. Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study.
Cited by 23 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Cayler cardiofacial syndrome and 22Q11 microdeletion with obstructed infracardiac total anomalous pulmonary venous connection (TAPVC) and hypoplastic aortic arch: A novel association;IHJ Cardiovascular Case Reports (CVCR);2020-09
2. The 22q11.2 Microdeletion in Pediatric Patients with Cleft Lip, Palate, or Both and Congenital Heart Disease: A Systematic Review;Journal of Pediatric Genetics;2019-10-23
3. Congenital unilateral hypoplasia of depressor anguli oris muscle in adult;Archives of Craniofacial Surgery;2019-08-20
4. Esophageal Atresia and Thenar Hypoplasia Associated with Asymmetric Crying Face;Journal of Pediatric Genetics;2019-04-01
5. What is new with 22q? An update from the 22q and You Center at the Children's Hospital of Philadelphia;American Journal of Medical Genetics Part A;2018-10
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