Dental and Maxillofacial Signs in Aarskog Syndrome: A Review of 3 Siblings and the Literature
Author:
Publisher
Elsevier BV
Subject
Otorhinolaryngology,Oral Surgery,Surgery
Reference22 articles.
1. A familial syndrome of short stature associated with facial dysplasia and genital anomalies;Aarskog;J Pediatr,1970
2. Unusual facies, joint hypermobility, genital anomaly and short stature: A new dysmorphic syndrome;Scott;Birth Defects Orig Artic Ser,1971
3. Isolation and characterization of the faciogenital dysplasia (Aarskog-Scott syndrome) gene: A putative Rho/Rac guanine nucleotide exchange factor;Pasteris;Cell,1994
4. Genomic organization of the faciogenital dysplasia (FGD1; Aarskog syndrome) gene;Pasteris;Genomics,1997
5. Clinical utility gene card for: Aarskog-Scott syndrome (faciogenital dysplasia)—Update 2015;Orrico;Eur J Hum Genet,2015
Cited by 3 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. A Novel Dental and Maxillofacial Sign in Aarskog Syndrome: A Family Case and Review of the Literature;Journal of Craniofacial Surgery Open;2024-03
2. Velopharyngeal Characteristics in Aarskog–Scott Syndrome: A Case Report;The Cleft Palate Craniofacial Journal;2022-12-06
3. Dental and maxillofacial features of Noonan Syndrome: Case series of ten patients;Journal of Cranio-Maxillofacial Surgery;2020-03
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