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ADAMTS19-associated heart valve defects: Novel genetic variants consolidating a recognizable cardiac phenotype.
Massadeh, Salam; Alhashem, Amal; van de Laar, Ingrid M B H; Alhabshan, Fahad; Ordonez, Natalia; Alawbathani, Salem; Khan, Suliman; Kabbani, Mohamed S; Chaikhouni, Farah; Sheereen, Atia; Almohammed, Iman; Alghamdi, Bader; Frohn-Mulder, Ingrid; Ahmad, Salim; Beetz, Christian; Bauer, Peter; Wessels, Marja W; Alaamery, Manal; Bertoli-Avella, Aida M.
Afiliación
  • Massadeh S; Department of Developmental Medicine, King Abdullah International Medical Research Center, King Saud Bin Abdulaziz University for Health Sciences, King Abdulaziz Medical City, Ministry of National Guard Health Affairs, Riyadh, Saudi Arabia.
  • Alhashem A; The Joint Center of Excellence for Biomedicine Between King Abdulaziz City for Science and Technology (KACST) and Brigham & Women's Hospital (BWH), Joint Centers of Excellence Program, King Abdulaziz City for Science and Technology (KACST), Riyadh, Saudi Arabia.
  • van de Laar IMBH; Division of Pediatric Genetics, Department of Pediatrics, Prince Sultan Military Medical City, Riyadh, Saudi Arabia.
  • Alhabshan F; Department of Anatomy and Cell biology, College of Medicine, Alfaisal University, Riyadh, Saudi Arabia.
  • Ordonez N; Department of Clinical Genetics, Erasmus University Medical Center, Rotterdam, The Netherlands.
  • Alawbathani S; Department of Cardiac Sciences, Ministry of the National Guard-Health Affairs, King Abdullah International Medical Research Center, King Saud bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia.
  • Khan S; CENTOGENE AG, Rostock, Germany.
  • Kabbani MS; CENTOGENE AG, Rostock, Germany.
  • Chaikhouni F; CENTOGENE AG, Rostock, Germany.
  • Sheereen A; Department of Cardiac Sciences, Ministry of the National Guard-Health Affairs, King Abdullah International Medical Research Center, King Saud bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia.
  • Almohammed I; Department of Cardiac Sciences, Ministry of the National Guard-Health Affairs, King Abdullah International Medical Research Center, King Saud bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia.
  • Alghamdi B; Department of Developmental Medicine, King Abdullah International Medical Research Center, King Saud Bin Abdulaziz University for Health Sciences, King Abdulaziz Medical City, Ministry of National Guard Health Affairs, Riyadh, Saudi Arabia.
  • Frohn-Mulder I; Department of Developmental Medicine, King Abdullah International Medical Research Center, King Saud Bin Abdulaziz University for Health Sciences, King Abdulaziz Medical City, Ministry of National Guard Health Affairs, Riyadh, Saudi Arabia.
  • Ahmad S; The Joint Center of Excellence for Biomedicine Between King Abdulaziz City for Science and Technology (KACST) and Brigham & Women's Hospital (BWH), Joint Centers of Excellence Program, King Abdulaziz City for Science and Technology (KACST), Riyadh, Saudi Arabia.
  • Beetz C; Department of Developmental Medicine, King Abdullah International Medical Research Center, King Saud Bin Abdulaziz University for Health Sciences, King Abdulaziz Medical City, Ministry of National Guard Health Affairs, Riyadh, Saudi Arabia.
  • Bauer P; Department of Pediatric Cardiology, Erasmus University Medical Center, Rotterdam, The Netherlands.
  • Wessels MW; Prince Sultan Cardiac Center, Prince Sultan Military Medical City, Riyad, Saudi Arabia.
  • Alaamery M; CENTOGENE AG, Rostock, Germany.
  • Bertoli-Avella AM; CENTOGENE AG, Rostock, Germany.
Clin Genet ; 98(1): 56-63, 2020 07.
Article en En | MEDLINE | ID: mdl-32323311
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Variación Genética / Proteínas ADAMTS / Cardiopatías Congénitas / Enfermedades de las Válvulas Cardíacas Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Child / Child, preschool / Female / Humans / Male Idioma: En Revista: Clin Genet Año: 2020 Tipo del documento: Article País de afiliación: Arabia Saudita
Texto completo
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Variación Genética / Proteínas ADAMTS / Cardiopatías Congénitas / Enfermedades de las Válvulas Cardíacas Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Child / Child, preschool / Female / Humans / Male Idioma: En Revista: Clin Genet Año: 2020 Tipo del documento: Article País de afiliación: Arabia Saudita