Otocephaly
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
General Medicine
Reference15 articles.
1. Agnathia, situs inversus, and associated malformations;Pauli;Teratology,1981
2. Familial agnathia– holoprosencephaly;Pauli;Am J Med Genet,1983
3. An anatomical study of human otocephaly;Lawrence;Teratology,1984
4. Familial agnathia–holoprosencephaly caused by an inherited unbalanced translocation and not autosomal recessive inheritance;Krassikoff;Am J Med Genet,1989
5. Prenatal diagnosis of otocephaly with microphthalmia/anophthalmia using ultrasound and magnetic resonance imaging;Chen;Ultrasound Obstet Gynecol,2003
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1. Otocephaly: Agnathia-Microstomia-Synotia Syndrome;International Journal of Infertility & Fetal Medicine;2021
2. Re-focusing on Agnathia-Otocephaly complex;Clinical Oral Investigations;2020-07-09
3. Cranial ultrasonographic findings in healthy full-term neonates: A retrospective review;Journal of the Chinese Medical Association;2012-08
4. Agnathia–otocephaly complex: A case report and examination of the OTX2 and PRRX1 genes;Gene;2012-02
5. Otocephaly: Prenatal and postnatal imaging findings;Journal of Pediatric Neurosciences;2011
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