المؤلفون: Krzyzewska, I. M., Maas, S. M., Henneman, Peter, Lip, K. V. D., Venema, A., Baranano, K., Chassevent, A., Aref-Eshghi, E., Essen, A. J. van, Fukuda, T., Ikeda, H., Jacquemont, M., Kim, H. G., Labalme, Audrey, Lewis, S. M., Lesca, Gaetan, Madrigal Bajo, Irene, Mahida, S., Matsumoto, N., Rabionet Janssen, Raquel, Rajcan-Separovic, E., Qiao, Y., Sadikovic, B., Saitsu, H., Sweetser, D. A., Alders, M., Mannens, M. M. A. M.

المصدر: Articles publicats en revistes (Genètica, Microbiologia i Estadística)

مصطلحات موضوعية: Expressió gènica, Malalties, Gene expression, Diseases

وصف الملف: 15 p.; application/pdf

العلاقة: Reproducció del document publicat a: https://doi.org/10.1186/s13148-019-0749-3Test; Clinical Epigenetics, 2019, vol. 11, p. 156; https://doi.org/10.1186/s13148-019-0749-3Test; info:eu-repo/grantAgreement/EC/FP7/223143/EU//TECHGENE; http://hdl.handle.net/2445/157659Test; 695988

الإتاحة: https://doi.org/10.1186/s13148-019-0749-3Test
http://hdl.handle.net/2445/157659Test

المؤلفون: Adadi, N., Lahrouchi, N., Bouhouch, R., Fellat, I., Amri, R., Alders, M., Sefiani, A., Bezzina, C., Ratbi, I.

المصدر: Journal of Medical Case Reports; 4/2/2017, Vol. 11, p1-5, 5p

مصطلحات موضوعية: JERVELL-Lange Nielsen syndrome, ION channels, RARE diseases, TACHYARRHYTHMIAS, GENETIC mutation

المؤلفون: Krzyzewska, I. M.¹ (AUTHOR), Alders, M.¹ (AUTHOR), Maas, S. M.² (AUTHOR), Bliek, J.¹ (AUTHOR), Venema, A.¹ (AUTHOR), Henneman, P.¹ (AUTHOR), Rezwan, F. I.³ (AUTHOR), Lip, K. v. d.¹ (AUTHOR), Mul, A. N.¹ (AUTHOR), Mackay, D. J. G.³ (AUTHOR), Mannens, M. M. A. M.¹ (AUTHOR) m.a.mannens@amc.uva.nl

المصدر: Clinical Epigenetics. 3/21/2019, Vol. 11 Issue 1, pN.PAG-N.PAG. 1p.

مصطلحات موضوعية: *DNA methylation, *METHYLATION, *MOLECULAR conformation, *SYNDROMES