1
2
Hofman, N., Jongbloed, R., Postema, P.G., Nannenberg, E., Alders, M., Wilde, A.A.M.
Veröffentlicht in: Hofman , N , Jongbloed , R , Postema , P G , Nannenberg , E , Alders , M & Wilde , A A M 2011 , ' Recurrent and Founder Mutations in the Netherlands: the Long-QT Syndrome ' , Cardiologie , vol. 19 , no. 1 , pp. 10-16 . https://doi.org/10.1007/s12471-010-0046-4;
2011
Veröffentlicht in: Hofman , N , Jongbloed , R , Postema , P G , Nannenberg , E , Alders , M & Wilde , A A M 2011 , ' Recurrent and Founder Mutations in the Netherlands: the Long-QT Syndrome ' , Cardiologie , vol. 19 , no. 1 , pp. 10-16 . https://doi.org/10.1007/s12471-010-0046-4;
2011
3
van den Wijngaard, A, Volders, P, Tintelen, JP, Jongbloed, JDH, Lambregtse - van den Berg, Mijke, Deprez, RHL, Mannens, MMAM, Hofmann, N, van Slegtenhorst, M, Dooijes, D, Michels, Michelle, Arens, Y, Jongbloed, R, Smeets, BJM
Veröffentlicht in: van den Wijngaard , A , Volders , P , Tintelen , JP , Jongbloed , JDH , Lambregtse - van den Berg , M , Deprez , RHL , Mannens , MMAM , Hofmann , N , van Slegtenhorst , M , Dooijes , D , Michels , M , Arens , Y , Jongbloed , R & Smeets , BJM 2011 , ' Recurrent and founder mutations in the Netherlands: cardiac Troponin I (TNNI3) gene mutations as a cause of severe forms of hypertrophic and restrictive cardiomyopathy ' , Netherlands Heart Journal , vol. 19 , no. 7-8 , pp. 344-351 . https://doi.org/10.1007/s12471-011-0135-z;
2011
Veröffentlicht in: van den Wijngaard , A , Volders , P , Tintelen , JP , Jongbloed , JDH , Lambregtse - van den Berg , M , Deprez , RHL , Mannens , MMAM , Hofmann , N , van Slegtenhorst , M , Dooijes , D , Michels , M , Arens , Y , Jongbloed , R & Smeets , BJM 2011 , ' Recurrent and founder mutations in the Netherlands: cardiac Troponin I (TNNI3) gene mutations as a cause of severe forms of hypertrophic and restrictive cardiomyopathy ' , Netherlands Heart Journal , vol. 19 , no. 7-8 , pp. 344-351 . https://doi.org/10.1007/s12471-011-0135-z;
2011
4
van den Wijngaard, A., Volders, P., Van Tintelen, J. P., Jongbloed, J. D. H., van den Berg, M. P., Deprez, R. H. Lekanne, Mannens, M. M. A. M., Hofmann, N., Slegtenhorst, M., Dooijes, D., Michels, M., Arens, Y., Jongbloed, R., Smeets, B. J. M.
Veröffentlicht in: van den Wijngaard , A , Volders , P , Van Tintelen , J P , Jongbloed , J D H , van den Berg , M P , Deprez , R H L , Mannens , M M A M , Hofmann , N , Slegtenhorst , M , Dooijes , D , Michels , M , Arens , Y , Jongbloed , R & Smeets , B J M 2011 , ' Recurrent and founder mutations in the Netherlands : cardiac Troponin I (TNNI3) gene mutations as a cause of severe forms of hypertrophic and restrictive cardiomyopathy ' , Netherlands Heart Journal , vol. 19 , no. 7-8 , pp. 344-351 . https://doi.org/10.1007/s12471-011-0135-z;
2011
Veröffentlicht in: van den Wijngaard , A , Volders , P , Van Tintelen , J P , Jongbloed , J D H , van den Berg , M P , Deprez , R H L , Mannens , M M A M , Hofmann , N , Slegtenhorst , M , Dooijes , D , Michels , M , Arens , Y , Jongbloed , R & Smeets , B J M 2011 , ' Recurrent and founder mutations in the Netherlands : cardiac Troponin I (TNNI3) gene mutations as a cause of severe forms of hypertrophic and restrictive cardiomyopathy ' , Netherlands Heart Journal , vol. 19 , no. 7-8 , pp. 344-351 . https://doi.org/10.1007/s12471-011-0135-z;
2011