Chromosome 12q24.31 microdeletion and congenital heart disease: a case report and review of the literature.

Bhatia, Neha S; Lim, Jiin-Ying; Brett, Maggie S; Tan, Ene-Choo; Law, Hai Yang; Thomas, Biju; Choo, Jonathan; Lai, Angeline H M; Jamuar, Saumya S

Bhatia, Neha S; Lim, Jiin-Ying; Brett, Maggie S; Tan, Ene-Choo; Law, Hai Yang; Thomas, Biju; Choo, Jonathan; Lai, Angeline H M; Jamuar, Saumya S.

Afiliación

Bhatia NS; Department of Paediatrics.
Lim JY; Department of Paediatrics.
Brett MS; KK Research Centre.
Tan EC; KK Research Centre.
Law HY; Paediatric Academic Clinical Programme, SingHealth Duke-NUS Medical School, Singapore, Singapore.
Thomas B; DNA Diagnostic and Research Laboratory.
Choo J; Paediatric Academic Clinical Programme, SingHealth Duke-NUS Medical School, Singapore, Singapore.
Lai AHM; Department of Paediatrics.
Jamuar SS; Paediatric Academic Clinical Programme, SingHealth Duke-NUS Medical School, Singapore, Singapore.

Clin Dysmorphol ; 28(1): 53-56, 2019 Jan.

Article en En | MEDLINE | ID: mdl-30507726

Asunto(s)

Cromosomas Humanos Par 12/genética; Cardiopatías Congénitas/genética; Preescolar; Deleción Cromosómica; Femenino; Eliminación de Gen; Humanos; Lactante; Masculino

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Cromosomas Humanos Par 12 / Cardiopatías Congénitas Límite: Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Clin Dysmorphol Asunto de la revista: TERATOLOGIA Año: 2019 Tipo del documento: Article

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