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

Por DABORA, S, NIETO, A, FRANZ, D, JOZWIAK, S, VAN DEN OUWELAND, A, KWIATKOWSKI, D
Publicado em 2000

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

Por Berns, A, van den Ouweland, A, Quint, W, van Oirschot, J, Gielkens, A
Publicado em 1985

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

Por Willemsen, R, Los, F, Mohkamsing, S, van den Ouweland, A, Deelen, W, Galjaard, H, Oostra, B
Publicado em 1997

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

Por LAAN, L, VAN DEN OUWELAND, A M W, BAKKER, P, HALLEY, D, CATSMAN-BERREVOET..., C
Publicado em 1999

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

Por Verbeek, J S, Roebroek, A J, van den Ouweland, A M, Bloemers, H P, Van de Ven, W J
Publicado em 1985

Nucleotide sequence analysis of the human fur gene.

Por Van den Ouweland, A M, Van Groningen, J J, Roebroek, A J, Onnekink, C, Van de Ven, W J
Publicado em 1989

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

Por Van den Ouweland, A M, van Groningen, J J, Hendriksen, P J, Bloemers, H P, Van de Ven, W J
Publicado em 1987

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

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

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

Por van Rijn, M A, de Vries, B B, Tibben, A, van den Ouweland, A M, Halley, D J, Niermeijer, M F
Publicado em 1997

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

Por Van den Ouweland, A M, Roebroek, A J, Schalken, J A, Claesen, C A, Bloemers, H P, Van de Ven, W J
Publicado em 1986

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

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

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

Por Van den Ouweland, A M, Van Duijnhoven, H L, Deichmann, K A, Van Groningen, J J, de Leij, L, Van de Ven, W J
Publicado em 1989

Genetic organization of the c-sis transcription unit.

Por Van den Ouweland, A M, Van Groningen, J J, Schalken, J A, Van Neck, H W, Bloemers, H P, Van de Ven, W J
Publicado em 1987

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

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

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

Por 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.
Publicado em 1999

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

Por 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
Publicado em 1998

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

Por 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
Publicado em 1997

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

Por 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
Publicado em 1998

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

Por 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.
Publicado em 1999

Two polymorphisms at the DXS539 locus

Por Van Den Hurk, J.A.J.M., Dreesen, J.C.F.M., Van Den Berg, H., Van Bennekom, C.A., Van Den Ouweland, A.M.W., Van Oost, B.A.
Publicado em 1991