Bosma arhinia microphthalmia syndrome: Clinical report and review of the literature-Reference-Cited by-同舟云学术

Bosma arhinia microphthalmia syndrome: Clinical report and review of the literature

Published:2016-02-03 Issue:5 Volume:170 Page:1302-1307
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Brasseur Benjamin¹,Martin Cindy M.²,Cayci Zuzan³,Burmeister Lynn²,Schimmenti Lisa A.⁴

Affiliation:

1. University of Minnesota Medical School; Minneapolis Minnesota

2. Department of Medicine; University of Minnesota; Minneapolis Minnesota

3. Department of Radiology; University of Minnesota; Minneapolis Minnesota

4. Department of Pediatrics; Ophthalmology and Vision Neuroscience, Genetics Cell Biology and Development; University of Minnesota; Minneapolis Minnesota

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference20 articles.

1. Congenital partial arhinia: A case report;Akkuzu;J Med Case Reports,2007

2. Bosma arrhinia microphthalmia syndrome in a Mexican patient with a molecular analysis of PAX6;Becerra-Solano;Clin Dysmorphol,2016

3. Hypoplasia of the nose and eyes, hyposmia, hypogeusia, and hypogonadotrophic hypogonadism in two males;Bosma;J Craniofac Genet Dev Biol,1981

4. Occurrence of complete arhinia in two siblings with a clinical picture of Treacher Collins syndrome negative for TCOF1, POLR1D and POLR1C mutations;Cesaretti;Clin Dysmorphol,2011

5. Arhinia revisited;Cohen;Rhinology,1987

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