Forensic medicine and the polymerase chain reaction technique.

Por Decorte, R, Cassiman, J J
Publicado em 1993

Quality issues in clinical genetic services

Por Kristoffersson, Ulf., Schmidtke, Jörg., Cassiman, J. J.
Publicado em 2010

Identification of internal variation in the pseudoautosomal VNTR DXYS17, with nonrandom distribution of the alleles on the X and the Y chromosomes.

Por Decorte, R., Wu, R., Marynen, P., Cassiman, J. J.
Publicado em 1994

Attitudes towards predictive testing in Huntington's disease: a recent survey in Belgium.

Por Evers-Kiebooms, G, Cassiman, J J, van den Berghe, H
Publicado em 1987

Rat hemoglobin interferes with DNA migration in agarose gels.

Por Deichmann, K, Marynen, P, Van den Berghe, H, Cassiman, J J
Publicado em 1988

MASA syndrome: new clinical features and linkage analysis using DNA probes.

Por Schrander-Stumpel, C, Legius, E, Fryns, J P, Cassiman, J J
Publicado em 1990

X linked mental retardation and infantile spasms in a family: new clinical data and linkage to Xp11.4-Xp22.11

Por Stromme, P., Sundet, K., Mork, C., Cassiman, J., Fryns, J., Claes, S.
Publicado em 1999

Incorporation of dITP or 7-deaza dGTP during PCR improves sequencing of the product.

Por Dierick, H, Stul, M, De Kelver, W, Marynen, P, Cassiman, J J
Publicado em 1993

X linked complicated spastic paraplegia, MASA syndrome, and X linked hydrocephalus owing to congenital stenosis of the aqueduct of Sylvius: variable expression of the same mutation...

Por Fryns, J P, Spaepen, A, Cassiman, J J, van den Berghe, H
Publicado em 1991

Relation of internal thioesters to conformational change and receptor-recognition site in alpha 2-macroglobulin complexes.

Por Van Leuven, F, Marynen, P, Cassiman, J J, Van den Berghe, H
Publicado em 1982

Lack of homozygotes for the most frequent disease allele in carbohydrate-deficient glycoprotein syndrome type 1A.

Por Matthijs, G, Schollen, E, Van Schaftingen, E, Cassiman, J J, Jaeken, J
Publicado em 1998

Linkage and association of the HLA gene complex with IDDM in 81 Danish families: strong linkage between DR beta 1Lys71+ and IDDM.

Por Zamani, M, Pociot, F, Spaepen, M, Raeymaekers, P, Nerup, J, Cassiman, J J
Publicado em 1996

Severe alport phenotype in a woman with two missense mutations in the same COL4A5 gene and preponderant inactivation of the X chromosome carrying the normal allele.

Por Guo, C, Van Damme, B, Vanrenterghem, Y, Devriendt, K, Cassiman, J J, Marynen, P
Publicado em 1995

Encephalocraniocutaneous lipomatosis with a mutation in the NF1 gene.

Por Legius, E, Wu, R, Eyssen, M, Marynen, P, Fryns, J P, Cassiman, J J
Publicado em 1995

A monoclonal antibody to the calmodulin-binding (Ca2+ + Mg2+)-dependent ATPase from pig stomach smooth muscle inhibits plasmalemmal (Ca2+ + Mg2+)-dependent ATPase activity.

Por Verbist, J, Wuytack, F, Raeymaekers, L, Van Leuven, F, Cassiman, J J, Casteels, R
Publicado em 1986

Identification of a 64 kDa heparan sulphate proteoglycan core protein from human lung fibroblast plasma membranes with a monoclonal antibody.

Por de Boeck, H, Lories, V, David, G, Cassiman, J J, van den Berghe, H
Publicado em 1987

Identification of cell surface dipeptidylpeptidase IV in human fibroblasts.

Por Saison, M, Verlinden, J, Van Leuven, F, Cassiman, J J, Van den Berghe, H
Publicado em 1983

Sister chromatid exchange induced by anti-herpes drugs.

Por Cassiman, J J, De Clercq, E, Jones, A S, Walker, R T, Van den Berghe, H
Publicado em 1981

MASA syndrome (a form of complicated spastic paraplegia) and X linked hydrocephalus: variable expression of the same mutation at Xq28? Call for families.

Por Schrander-Stumpel, C, Fryns, J, Cassiman, J J, Legius, E, Spaepen, A, Höweler, C J
Publicado em 1992

Localisation of a new gene for non-specific mental retardation to Xq22-q26 (MRX35).

Por Gu, X X, Decorte, R, Marynen, P, Fryns, J P, Cassiman, J J, Raeymaekers, P
Publicado em 1996