A new frontonasal dysplasia syndrome associated with deletion of the SIX2 gene.
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| Title: | A new frontonasal dysplasia syndrome associated with deletion of the SIX2 gene. |
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| Authors: | Hufnagel RB; Division of Human Genetics, Cincinnati Children's Hospital Medical Center and Department of Pediatrics. University of Cincinnati College of Medicine, Cincinnati, Ohio., Zimmerman SL; Division of Human Genetics, Cincinnati Children's Hospital Medical Center and Department of Pediatrics. University of Cincinnati College of Medicine, Cincinnati, Ohio., Krueger LA; Division of Human Genetics, Cincinnati Children's Hospital Medical Center and Department of Pediatrics. University of Cincinnati College of Medicine, Cincinnati, Ohio., Bender PL; Division of Human Genetics, Cincinnati Children's Hospital Medical Center and Department of Pediatrics. University of Cincinnati College of Medicine, Cincinnati, Ohio., Ahmed ZM; Department of Otorhinolaryngology, University of Maryland, Baltimore, Maryland., Saal HM; Division of Human Genetics, Cincinnati Children's Hospital Medical Center and Department of Pediatrics. University of Cincinnati College of Medicine, Cincinnati, Ohio. |
| Source: | American journal of medical genetics. Part A [Am J Med Genet A] 2016 Feb; Vol. 170A (2), pp. 487-491. Date of Electronic Publication: 2015 Nov 18. |
| Publication Type: | Case Reports; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't |
| Journal Info: | Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235741 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1552-4833 (Electronic) Linking ISSN: 15524825 NLM ISO Abbreviation: Am J Med Genet A Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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| ISSN: | 1552-4833 |
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| DOI: | 10.1002/ajmg.a.37441 |
