Otocephaly: Agnathia-Microstomia-Synotia Syndrome
Author:
Publisher
Jaypee Brothers Medical Publishing
Subject
Reproductive Medicine
Link
https://www.ijifm.com/doi/pdf/10.5005/jp-journals-10016-1195
Reference16 articles.
1. 1. Hwang K-S, Ding D-C, Chang Y-K, et al. Otocephaly. Chin Med Assoc 2007;70(7):298–301. DOI: 10.1016/S1726-4901(07)70009-6.
2. 2. Gekas J, Li B, Kamnasaran D. Current perspectives on the etiology of agnathia-otocephaly. Eur J Med Genet 2010;53(6):358–366. DOI: 10.1016/j.ejmg.2010.09.002.
3. 3. Krassikoff N, Sekhon GS. Familial agnathia–holoprosencephaly caused by an inherited unbalanced translocation and not autosomal recessive inheritance. Am J Med Genet 1989;34(2):255–257. DOI: 10.1002/ajmg.1320340227.
4. 4. Faye-Petersen O, David E, Rangwala N, et al. Otocephaly: report of five new cases and a literature review. Fetal Pediatr Pathol 2006;25(5):277–296. DOI: 10.1080/15513810601123417.
5. 5. Ibba RM, Zoppi MA, Floris M, et al. Otocephaly: prenatal diagnosis of a new case and etiopathogenetic considerations. Am J Med Genet 2000;90(5):427–429. DOI: 10.1002/(SICI)1096-8628(20000228)90:5427::AID-AJMG133.0.CO;2-5.
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