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X-linked myxomatous valvular dystrophy in a patient with a novel mutation in the FLNA gene.
Madej-Pilarczyk, Agnieszka; Piekutowska-Abramczuk, Dorota; Kucinska, Beata; Furmanek, Mariusz; Gwiazda, Anna; Ciara, Elzbieta; Chrzanowska, Krystyna H; Werner, Bozena.
Afiliação
  • Madej-Pilarczyk A; Department of Medical Genetics, The Children's Memorial Health Institute, Warszawa, Poland. a.madej-pilarczyk@ipczd.pl.
  • Piekutowska-Abramczuk D; Department of Medical Genetics, The Children's Memorial Health Institute, Warszawa, Poland.
  • Kucinska B; Department of Pediatric Cardiology and General Pediatrics, Medical University of Warsaw, Warszawa, Poland.
  • Furmanek M; Department of Pediatric Radiology, Medical University of Warsaw, Warszawa, Poland.
  • Gwiazda A; Department of Pediatric Radiology, Medical University of Warsaw, Warszawa, Poland.
  • Ciara E; Department of Medical Genetics, The Children's Memorial Health Institute, Warszawa, Poland.
  • Chrzanowska KH; Department of Medical Genetics, The Children's Memorial Health Institute, Warszawa, Poland.
  • Werner B; Department of Pediatric Cardiology and General Pediatrics, Medical University of Warsaw, Warszawa, Poland.
Kardiol Pol ; 81(3): 306-307, 2023.
Article em En | MEDLINE | ID: mdl-36640296
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Prolapso da Valva Mitral / Doenças Genéticas Ligadas ao Cromossomo X / Cardiopatias Congênitas Limite: Humans Idioma: En Revista: Kardiol Pol Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Polônia
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Prolapso da Valva Mitral / Doenças Genéticas Ligadas ao Cromossomo X / Cardiopatias Congênitas Limite: Humans Idioma: En Revista: Kardiol Pol Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Polônia