Large deletion causing the TSC2-PKD1 contiguous gene syndrome without infantile polycystic disease

per Smulders, Y, Eussen, B, Verhoef, S, Wouters, C
Publicat 2003

Segregation of FRAXE in a large family: clinical, psychometric, cytogenetic, and molecular data.

per Hamel, B. C., Smits, A. P., de Graaff, E., Smeets, D. F., Schoute, F., Eussen, B. H., Knight, S. J., Davies, K. E., Assman-Hulsmans, C. F., Oostra, B. A.
Publicat 1994

Nimbus: a design-driven analyses suite for amplicon-based NGS data

per Brouwer, R W W, van den Hout, M C G N, Kockx, C E M, Brosens, E, Eussen, B, de Klein, A, Sleutels, F, van IJcken, W F J
Publicat a Bioinformatics (2018)

An unbalanced submicroscopic translocation t(8;16)(q24.3;p13.3)pat associated with tuberous sclerosis complex, adult polycystic kidney disease, and hypomelanosis of Ito

per Eussen, B., Bartalini, G., Bakker, L., Balestri, P., Di, L, Van Hemel, J. O, Dauwerse, H., van den Ouweland, A. M W, Ris-Stalpers, C., Verhoef, S., Halley, D., Fois, A.
Publicat 2000

X chromosome inactivation in a female carrier of a 1.28 Mb deletion encompassing the human X inactivation centre

per de Hoon, B., Splinter, Erik, Eussen, B., Douben, J. C. W., Rentmeester, E., van de Heijning, M., Laven, J. S. E., de Klein, J. E. M. M., Liebelt, J., Gribnau, J.
Publicat a Philos Trans R Soc Lond B Biol Sci (2017)

Molecular cytogenetic analysis of eight inversion duplications of human chromosome 13q that each contain a neocentromere.

per Warburton, P E, Dolled, M, Mahmood, R, Alonso, A, Li, S, Naritomi, K, Tohma, T, Nagai, T, Hasegawa, T, Ohashi, H, Govaerts, L C, Eussen, B H, Van Hemel , J O, Lozzio, C, Schwartz, S, Dowhanick-Morrissette, J J, Spinner, N B, Rivera, H, Crolla, J A, Yu, C, Warburton, D
Publicat 2000

Distinctive Phenotypic Abnormalities Associated with Submicroscopic 21q22 Deletion Including DYRK1A

per Oegema, R., de Klein, A., Verkerk, A.J., Schot, R., Dumee, B., Douben, H., Eussen, B., Dubbel, L., Poddighe, P.J., van der Laar, I., Dobyns, W.B., van der Spek, P.J., Lequin, M.H., de Coo, I.F.M., de Wit, M.-C.Y., Wessels, M.W., Mancini, G.M.S.
Publicat 2010