The effect of a single base pair deletion (delta T525) and a C1634T missense mutation (pro545leu) on the expression of lysosomal alpha-glucosidase in patients with glycogen storage disease type II
Hermans, M M, De Graaff, E, Kroos, M A, Mohkamsing, S, Eussen, B J, Joosse, M, Willemsen, R, Kleijer, W J, Oostra, B A, Reuser, A J
Published in Human molecular genetics (01.12.1994)
Published in Human molecular genetics (01.12.1994)
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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
Eussen, Bert H J, Bartalini, Gabriella, Bakker, Lida, Balestri, Paolo, Di Lucca, Carmela, Van Hemel, Jan O, Dauwerse, Hans, van den Ouweland, Ans M W, Ris-Stalpers, Carrie, Verhoef, Senno, Halley, Dicky J J, Fois, Alberto
Published in Journal of medical genetics (01.04.2000)
Published in Journal of medical genetics (01.04.2000)
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Identification of a homozygous deletion at 8p12-21 in a human prostate cancer xenograft
Van Alewijk, Dirk C., Van Der Weiden, Marcel M., Eussen, Bert J., Van Den Andel-Thijssen, Lydia D., Ehren-Van Eekelen, Conny C., König, Josée J., Van Steenbrugge, Gert J., Dinjens, Winand N., Trapman, Jan
Published in Genes chromosomes & cancer (01.02.1999)
Published in Genes chromosomes & cancer (01.02.1999)
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Large deletion causing the TSC2-PKD1 contiguous gene syndrome without infantile polycystic disease
Smulders, Y M, Eussen, B H J, Verhoef, S, Wouters, C H
Published in Journal of medical genetics (01.02.2003)
Published in Journal of medical genetics (01.02.2003)
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The murine CYLN2 gene : Genomic organization, chromosome localization, and comparison to the human gene that is located within the 7q11.23 Williams syndrome critical region
HOOGENRAAD, C. C, EUSSEN, B. H. J, LANGEVELD, A, VAN HAPEREN, R, WINTERBERG, S, WOUTERS, C. H, GROSVELD, F, DE ZEEUW, C. I, GALJART, N
Published in Genomics (San Diego, Calif.) (01.11.1998)
Published in Genomics (San Diego, Calif.) (01.11.1998)
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A novel gene on human chromosome 2p24 is differentially expressed between androgen-dependent and androgen-independent prostate cancer cells
Chang, G.T.G., Steenbeek, M., Schippers, E., Blok, L.J., van Weerden, W.M., van Alewijk, D.C.J.G., Eussen, B.H.J., van Steenbrugge, G.J., Brinkmann, A.O.
Published in European journal of cancer (1990) (01.11.2001)
Published in European journal of cancer (1990) (01.11.2001)
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Identification of a gene on human chromosome 8q11 that is differentially expressed during prostate‐cancer progression
Chang, Glenn T.G., Tapsi, Nita, Steenbeek, Martine, Blok, Leen J., van Weerden, Wytske M., van Alewijk, Dirk C.J.G., Eussen, Bert H.J., van Steenbrugge, Gert J., Brinkmann, Albert O.
Published in International journal of cancer (12.11.1999)
Published in International journal of cancer (12.11.1999)
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Deletions at chromosome regions 7q11.23 and 7q36 in a patient with Williams syndrome
Wouters, C H, Meijers-Heijboer, H J, Eussen, B J, van der Heide, A A, van Luijk, R B, van Drunen, E, Beverloo, B B, Visscher, F, Van Hemel, J O
Published in American journal of medical genetics (15.08.2001)
Published in American journal of medical genetics (15.08.2001)
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Submicroscopic Xpter deletion in a boy with growth and mental retardation caused by a familial t(X;14)
de Vries, B B, Eussen, B H, van Diggelen, O P, van Der Heide, A, Deelen, W H, Govaerts, L C, Lindhout, D, Wouters, C H, Van Hemel, J O
Published in American journal of medical genetics (19.11.1999)
Published in American journal of medical genetics (19.11.1999)
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