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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.
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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  Data: A new frontonasal dysplasia syndrome associated with deletion of the SIX2 gene.
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  Data: <searchLink fieldCode="AU" term="%22Hufnagel+RB%22">Hufnagel RB</searchLink>; Division of Human Genetics, Cincinnati Children's Hospital Medical Center and Department of Pediatrics. University of Cincinnati College of Medicine, Cincinnati, Ohio.<br /><searchLink fieldCode="AU" term="%22Zimmerman+SL%22">Zimmerman SL</searchLink>; Division of Human Genetics, Cincinnati Children's Hospital Medical Center and Department of Pediatrics. University of Cincinnati College of Medicine, Cincinnati, Ohio.<br /><searchLink fieldCode="AU" term="%22Krueger+LA%22">Krueger LA</searchLink>; Division of Human Genetics, Cincinnati Children's Hospital Medical Center and Department of Pediatrics. University of Cincinnati College of Medicine, Cincinnati, Ohio.<br /><searchLink fieldCode="AU" term="%22Bender+PL%22">Bender PL</searchLink>; Division of Human Genetics, Cincinnati Children's Hospital Medical Center and Department of Pediatrics. University of Cincinnati College of Medicine, Cincinnati, Ohio.<br /><searchLink fieldCode="AU" term="%22Ahmed+ZM%22">Ahmed ZM</searchLink>; Department of Otorhinolaryngology, University of Maryland, Baltimore, Maryland.<br /><searchLink fieldCode="AU" term="%22Saal+HM%22">Saal HM</searchLink>; Division of Human Genetics, Cincinnati Children's Hospital Medical Center and Department of Pediatrics. University of Cincinnati College of Medicine, Cincinnati, Ohio.
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  Data: <searchLink fieldCode="JN" term="%22101235741%22">American journal of medical genetics. Part A</searchLink> [Am J Med Genet A] 2016 Feb; Vol. 170A (2), pp. 487-491. <i>Date of Electronic Publication: </i>2015 Nov 18.
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        Value: 10.1002/ajmg.a.37441
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              Text: 2016 Feb
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