Forensic medicine and the polymerase chain reaction technique.

le Decorte, R, Cassiman, J J
Foilsithe 1993

Quality issues in clinical genetic services

le Kristoffersson, Ulf., Schmidtke, Jörg., Cassiman, J. J.
Foilsithe 2010

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

le Decorte, R., Wu, R., Marynen, P., Cassiman, J. J.
Foilsithe 1994

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

le Evers-Kiebooms, G, Cassiman, J J, van den Berghe, H
Foilsithe 1987

Rat hemoglobin interferes with DNA migration in agarose gels.

le Deichmann, K, Marynen, P, Van den Berghe, H, Cassiman, J J
Foilsithe 1988

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

le Schrander-Stumpel, C, Legius, E, Fryns, J P, Cassiman, J J
Foilsithe 1990

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

le Dierick, H, Stul, M, De Kelver, W, Marynen, P, Cassiman, J J
Foilsithe 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...

le Fryns, J P, Spaepen, A, Cassiman, J J, van den Berghe, H
Foilsithe 1991

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

le Van Leuven, F, Marynen, P, Cassiman, J J, Van den Berghe, H
Foilsithe 1982

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

le Matthijs, G, Schollen, E, Van Schaftingen, E, Cassiman, J J, Jaeken, J
Foilsithe 1998

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

le Zamani, M, Pociot, F, Spaepen, M, Raeymaekers, P, Nerup, J, Cassiman, J J
Foilsithe 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.

le Guo, C, Van Damme, B, Vanrenterghem, Y, Devriendt, K, Cassiman, J J, Marynen, P
Foilsithe 1995

Encephalocraniocutaneous lipomatosis with a mutation in the NF1 gene.

le Legius, E, Wu, R, Eyssen, M, Marynen, P, Fryns, J P, Cassiman, J J
Foilsithe 1995

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

le Verbist, J, Wuytack, F, Raeymaekers, L, Van Leuven, F, Cassiman, J J, Casteels, R
Foilsithe 1986

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

le de Boeck, H, Lories, V, David, G, Cassiman, J J, van den Berghe, H
Foilsithe 1987

Identification of cell surface dipeptidylpeptidase IV in human fibroblasts.

le Saison, M, Verlinden, J, Van Leuven, F, Cassiman, J J, Van den Berghe, H
Foilsithe 1983

Sister chromatid exchange induced by anti-herpes drugs.

le Cassiman, J J, De Clercq, E, Jones, A S, Walker, R T, Van den Berghe, H
Foilsithe 1981

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

le Schrander-Stumpel, C, Fryns, J, Cassiman, J J, Legius, E, Spaepen, A, Höweler, C J
Foilsithe 1992

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

le Gu, X X, Decorte, R, Marynen, P, Fryns, J P, Cassiman, J J, Raeymaekers, P
Foilsithe 1996

Prader-Willi syndrome in a child with mosaic trisomy 15 and mosaic triplo-X: a molecular analysis.

le Devriendt, K, Matthijs, G, Claes, S, Legius, E, Proesmans, W, Cassiman, J J, Fryns, J P
Foilsithe 1997