Report of a Family with Craniofrontonasal Syndrome and Wolff-Parkinson-White Syndrome: Is it a New Finding?

Kilit, Celal; Kilit, Türkan Pasali

Report of a Family with Craniofrontonasal Syndrome and Wolff-Parkinson-White Syndrome: Is it a New Finding? / Relato de uma Família com Síndrome Craniofrontonasal e Síndrome de Wolff-Parkinson-White: É um Novo Achado?

Kilit, Celal; Kilit, Türkan Pasali.

Kilit, Celal; Dumlupinar University. Faculty of Medicine. Department of Cardiology. Kütahya. TR
Kilit, Türkan Pasali; Dumlupinar University. Faculty of Medicine. Department of Internal Medicine. Kütahya. TR

Arq. bras. cardiol ; 112(5): 594-596, May 2019. graf

Article in English | LILACS | ID: biblio-1011202

Subject(s)

Humans; Female; Adolescent; Wolff-Parkinson-White Syndrome/genetics; Craniofacial Abnormalities/genetics; Wolff-Parkinson-White Syndrome/complications; Craniofacial Abnormalities/complications

Anormalidades Craniofaciais; Comparative Studies; Craniofacial Abnormalities; Craniofacial Dysostose; Estudos Comparativos; Hereditariedade; Síndrome de Wolff-Parkinson-White; Tachycardia, Supraventricular; Taquicardia Supraventricular; Wolff-Parkinson White Syndrome

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Full text: Available Index: LILACS (Americas) Main subject: Wolff-Parkinson-White Syndrome / Craniofacial Abnormalities Type of study: Diagnostic study Limits: Adolescent / Female / Humans Language: English Journal: Arq. bras. cardiol Journal subject: Cardiology Year: 2019 Type: Article Affiliation country: Turkey Institution/Affiliation country: Dumlupinar University/TR

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