A genetic assay of three patients in the same family with Holt-Oram syndrome; a case report.

Ebrahimzadeh-Vesal, Reza; Hosseini, Seyed Kianush; Rezakhanlu, Fereshteh; Derakhshandeh-Peykar, Pupak

Ebrahimzadeh-Vesal, Reza; Hosseini, Seyed Kianush; Rezakhanlu, Fereshteh; Derakhshandeh-Peykar, Pupak.

Afiliación

Ebrahimzadeh-Vesal R; Department of Medical Genetics, Medical Sciences, University of Tehran, Iran.
Hosseini SK; Tehran Heart Center, Medical Sciences, University of Tehran, Iran.
Rezakhanlu F; Tehran Heart Center, Medical Sciences, University of Tehran, Iran.
Derakhshandeh-Peykar P; Department of Medical Genetics, Medical Sciences, University of Tehran, Iran ; Medizinisch Genetisches Zentrum (MGZ), Munich, Germany.

Rep Biochem Mol Biol ; 2(1): 52-5, 2013 Oct.

Article en En | MEDLINE | ID: mdl-26989721

Palabras clave

Congenital heart malformation; Holt-Oram syndrome; TBX5 gene

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Rep Biochem Mol Biol Año: 2013 Tipo del documento: Article País de afiliación: Irán Pais de publicación: Irán

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