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DLG2 intragenic exonic deletions reinforce the link to neurodevelopmental disorders and suggest a potential association with congenital anomalies and dysmorphism.
Chen, Yunjia; Karaca, Ender; Robin, Nathaniel H; Goodloe, Dana; Al-Beshri, Ali; Dean, S Joy; Hurst, Anna C E; Carroll, Andrew J; Mikhail, Fady M.
Afiliación
  • Chen Y; Department of Genetics, University of Alabama at Birmingham, Birmingham, AL.
  • Karaca E; Department of Pathology, Baylor University Medical Center, Dallas, TX; Texas A&M School of Medicine, Dallas, TX.
  • Robin NH; Department of Genetics, University of Alabama at Birmingham, Birmingham, AL.
  • Goodloe D; Department of Genetics, University of Alabama at Birmingham, Birmingham, AL.
  • Al-Beshri A; Department of Genetics, University of Alabama at Birmingham, Birmingham, AL.
  • Dean SJ; Department of Genetics, University of Alabama at Birmingham, Birmingham, AL.
  • Hurst ACE; Department of Genetics, University of Alabama at Birmingham, Birmingham, AL.
  • Carroll AJ; Department of Genetics, University of Alabama at Birmingham, Birmingham, AL.
  • Mikhail FM; Department of Genetics, University of Alabama at Birmingham, Birmingham, AL. Electronic address: fmikhail@uab.edu.
Genet Med ; 26(1): 101010, 2024 Jan.
Article en En | MEDLINE | ID: mdl-37860969
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Trastornos del Neurodesarrollo Límite: Humans Idioma: En Revista: Genet Med Asunto de la revista: GENETICA MEDICA Año: 2024 Tipo del documento: Article País de afiliación: Albania Pais de publicación: Estados Unidos
Texto completo
Añadir a Mi BVS
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XML
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Trastornos del Neurodesarrollo Límite: Humans Idioma: En Revista: Genet Med Asunto de la revista: GENETICA MEDICA Año: 2024 Tipo del documento: Article País de afiliación: Albania Pais de publicación: Estados Unidos