المؤلفون: McMullan, D.J., Bonin, M., Hehir-Kwa, J.Y., Vries, L.B.A. de, Dufke, A., Rattenberry, E., Steehouwer, M., Moruz, L.M., Pfundt, R.P., Leeuw, N. de, Riess, A., Altug-Teber, O., Enders, H., Singer, S., Grasshoff, U., Walter, M., Walker, J.M., Lamb, C.V., Davison, E.V., Brueton, L., Riess, O., Veltman, J.A.

المصدر: Human Mutation, 30, 7, pp. 1082-92

مصطلحات موضوعية: IGMD 3: Genomic disorders and inherited multi-system disorders, NCMLS 6: Genetics and epigenetic pathways of disease, ONCOL 3: Translational research

Relation: http://hdl.handle.net/2066/79652

الاتاحة: http://hdl.handle.net/2066/79652
https://doi.org/10.1002/humu.21015