The KBG syndrome: Case report
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Medicine
Link
http://link.springer.com/content/pdf/10.1186/1757-1626-1-186.pdf
Reference8 articles.
1. Dowling PA, Fleming P, Gorlin RJ, King M, Nevin NC, McEntargart : The KBG syndrome, characteristic dental findings: a case report. International Journal of Pediatric Dentistry. 2001, 11: 131-134. 10.1046/j.1365-263x.2001.00231.x.
2. Zollino M, Battaglia A, D'Avanzo MG, Della Bruna MM, Marini G, Scarano G, Cappa M: Six additional cases of the KBG syndrome: clinical reports and outline of the diagnostic criteria. Am J Med Genet. 1994, 52: 302-307. 10.1002/ajmg.1320520310.
3. Soekarman D, Volcke P, Fryns JP: The KBG syndrome: follow-up data on three affected brothers. Clin Genet. 1994, 46: 283-286.
4. Fryns JP, Haspeslag M: Mental retardation, short stature, minor skeletal anomalies, craniofacial dysmorphism and macrodontia in two sisters and their mother: another variant example of the KBG syndrome?. Clin Genet. 1984, 26: 69-72.
5. Devriendt K, Holvoet M, Fryns JP: Further delineation of the KBG syndrome [abstract]. Genet Couns. 1998, 9 (3): 191-194.
Cited by 2 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. Audiological phenotyping evaluation in KBG syndrome: Description of a multicenter review;International Journal of Pediatric Otorhinolaryngology;2023-08
2. Congenital heart defects in molecularly confirmed KBG syndrome patients;American Journal of Medical Genetics Part A;2021-12-31
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