Author:
Kana M. A.,Baduku T. S.,Bello-Manga H.,Baduku A. S.
Publisher
Springer Science and Business Media LLC
Reference12 articles.
1. Lumaka A, Mubungu G, Mukaba P, Mutantu P, Luyeye G, Corveleyn A, Tady BP, Lukusa Tshilobo P, Devriendt K. A novel heterozygous mutation of three consecutive nucleotides causing Apert syndrome in a Congolese family. Eur. J. Med. Genet. 2014;57(4):169–73.
2. Tartaglia NR, Howell S, Sutherland A, Wilson R, Wilson L. A review of trisomy X (47,XXX). Orphanet J. Rare Dis. 2010;5:8.
3. Batra P, Duggal R, Parkash H. Dentofacial characteristics in Apert syndrome: a case report. J. Indian Soc. Pedod. Prev. Dent. 2002;20(3):118–23.
4. Bhatia PV, Patel PS, Jani YV, Soni NC. Apert's syndrome: Report of a rare case. J Oral Maxillofac Pathol. 2013;17(2):294–7.
5. Ofodile FA, Adeloye A. Acrocephalosyndactyly with hydrocephalus and dextrocardia in a Nigerian child. J Natl Med Assoc. 1982;74(8):800–3.
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