Characterisation of six large deletions in TSC2 identified using long range PCR suggests diverse mechanisms including Alu mediated recombination

od DABORA, S, NIETO, A, FRANZ, D, JOZWIAK, S, VAN DEN OUWELAND, A, KWIATKOWSKI, D
Wydane 2000

Presence of markers for virulence in the unique short region or repeat region or both of pseudorabies hybrid viruses.

od Berns, A, van den Ouweland, A, Quint, W, van Oirschot, J, Gielkens, A
Wydane 1985

Rapid antibody test for prenatal diagnosis of fragile X syndrome on amniotic fluid cells: a new appraisal.

od Willemsen, R, Los, F, Mohkamsing, S, van den Ouweland, A, Deelen, W, Galjaard, H, Oostra, B
Wydane 1997

Angelman syndrome: AS phenotype correlated with specific EEG pattern may result in a high detection rate of mutations in the UBE3A gene

od LAAN, L, VAN DEN OUWELAND, A M W, BAKKER, P, HALLEY, D, CATSMAN-BERREVOET..., C
Wydane 1999

Human c-fms proto-oncogene: comparative analysis with an abnormal allele.

od Verbeek, J S, Roebroek, A J, van den Ouweland, A M, Bloemers, H P, Van de Ven, W J
Wydane 1985

Nucleotide sequence analysis of the human fur gene.

od Van den Ouweland, A M, Van Groningen, J J, Roebroek, A J, Onnekink, C, Van de Ven, W J
Wydane 1989

Nucleotide sequence of the DNA region immediately upstream of the human c-sis proto-oncogene.

od Van den Ouweland, A M, van Groningen, J J, Hendriksen, P J, Bloemers, H P, Van de Ven, W J
Wydane 1987

Structural homology between the human fur gene product and the subtilisin-like protease encoded by yeast KEX2.

od van den Ouweland, A M, van Duijnhoven, H L, Keizer, G D, Dorssers, L C, Van de Ven, W J
Wydane 1990

DNA testing for fragile X syndrome: implications for parents and family.

od van Rijn, M A, de Vries, B B, Tibben, A, van den Ouweland, A M, Halley, D J, Niermeijer, M F
Wydane 1997

Structure and nucleotide sequence of the 5' region of the human and feline c-sis proto-oncogenes.

od Van den Ouweland, A M, Roebroek, A J, Schalken, J A, Claesen, C A, Bloemers, H P, Van de Ven, W J
Wydane 1986

A unique case of two somatic APC mutations in an early onset cribriform-morular variant of papillary thyroid carcinoma and overview of the literature

od Aydemirli, M. D., van der Tuin, K., Hes, F. J., van den Ouweland, A. M. W., van Wezel, T., Kapiteijn, E., Morreau, H.
Wydane w Fam Cancer (2019)

The structure of the human c-fes/fps proto-oncogene.

od Roebroek, A J, Schalken, J A, Verbeek, J S, Van den Ouweland, A M, Onnekink, C, Bloemers, H P, Van de Ven, W J
Wydane 1985

Characteristics of a multicopy gene family predominantly consisting of processed pseudogenes.

od Van den Ouweland, A M, Van Duijnhoven, H L, Deichmann, K A, Van Groningen, J J, de Leij, L, Van de Ven, W J
Wydane 1989

Genetic organization of the c-sis transcription unit.

od Van den Ouweland, A M, Van Groningen, J J, Schalken, J A, Van Neck, H W, Bloemers, H P, Van de Ven, W J
Wydane 1987

Familial translocations involving 15q11-q13 can give rise to interstitial deletions causing Prader-Willi or Angelman syndrome.

od Horsthemke, B, Maat-Kievit, A, Sleegers, E, van den Ouweland, A, Buiting, K, Lich, C, Mollevanger, P, Beverstock, G, Gillessen-Kaesbach, G, Schwanitz, G
Wydane 1996

Mutational spectrum of the TSC1 gene in a cohort of 225 tuberous sclerosis complex patients: no evidence for genotype-phenotype correlation

od van Slegtenhorst, M., Verhoef, S., Tempelaars, A., Bakker, L., Wang, Q., Wessels, M., Bakker, R., Nellist, M., Lindhout, D., Halley, D., van den Ouweland, A.
Wydane 1999

Familial cylindromatosis mimicking tuberous sclerosis complex and confirmation of the cylindromatosis locus, CYLD1, in a large family.

od Verhoef, S, Schrander-Stumpel, C T, Vuzevski, V D, Tempelaars, A, Jansen, L A, Malfeyt, G A, Ceelen, T L, Lindhout, D, Halley, D J, van den Ouweland, A M
Wydane 1998

Prenatal diagnosis of the fragile X syndrome: loss of mutation owing to a double recombinant or gene conversion event at the FMR1 locus.

od Losekoot, M, Hoogendoorn, E, Olmer, R, Jansen, C C, Oosterwijk, J C, van den Ouweland, A M, Halley, D J, Warren, S T, Willemsen, R, Oostra, B A, Bakker, E
Wydane 1997

A prospective 10 year follow up study of patients with neurofibromatosis type 1

od Cnossen, M, de Goede-Bolder, A, van den Broek, K M, Waasdorp, C, Oranje, A, Stroink, H, Simonsz, H, van den Ouweland, A M W, Halley, D, Niermeijer, M
Wydane 1998

Screening for the fragile X syndrome among the mentally retarded: a clinical study

od de Vries, B. B A, Mohkamsing, S., van den Ouweland, A. M W, Mol, E., Gelsema, K., van Rijn, M., Tibben, A., Halley, D., Duivenvoorden, H., Oostra, B., Niermeijer, M.
Wydane 1999