Two polymorphic loci are detected simultaneously by probe CARLP II8.2 [D10S21] on chromosome 10.

Por Raeymaekers, P, Van Broeckhoven, C, Vandenberghe, A
Publicado em 1988

A highly polymorphic locus is detected by probe CARLP II6.3 [D5S88]

Por Raeymaekers, P, Van Broeckhoven, C, Vandenberghe, A
Publicado em 1988

A polymorphic locus [D1S88] is detected by probe LA01.41 on chromosome 1p.

Por Raeymaekers, P, Van Broeckhoven, C, Vandenberghe, A
Publicado em 1989

A new gene (DYX3) for dyslexia is located on chromosome 2

Por Fagerheim, T., Raeymaekers, P., Tonnessen, F. E., Pedersen, M., Tranebjarg, L., Lubs, H.
Publicado em 1999

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

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

Estimation of the size of the chromosome 17p11.2 duplication in Charcot-Marie-Tooth neuropathy type 1a (CMT1a). HMSN Collaborative Research Group.

Por Raeymaekers, P, Timmerman, V, Nelis, E, Van Hul, W, De Jonghe, P, Martin, J J, Van Broeckhoven, C
Publicado em 1992

CAG repeat expansions in bipolar and unipolar disorders.

Por Oruc, L, Lindblad, K, Verheyen, G R, Ahlberg, S, Jakovljević, M, Ivezić, S, Raeymaekers, P, Van Broeckhoven, C, Schalling, M
Publicado em 1997

Homozygosity mapping to the USH2A locus in two isolated populations

Por Fagerheim, T, Raeymaekers, P, Merren, J, Mani, K, Jha, G, Baumbach, L, Brox, V, Breines, E, Holdo, B, Holdo, A, Tranebjarg, L
Publicado em 1999

Localization of the mutation in an extended family with Charcot-Marie-Tooth neuropathy (HMSN I).

Por Raeymaekers, P, Timmerman, V, De Jonghe, P, Swerts, L, Gheuens, J, Martin, J J, Muylle, L, De Winter, G, Vandenberghe, A, Van Broeckhoven, C
Publicado em 1989

Assignment of the Charcot-Marie-Tooth neuropathy type 1 (CMT 1a) gene to 17p11.2-p12.

Por Timmerman, V, Raeymaekers, P, De Jonghe, P, De Winter, G, Swerts, L, Jacobs, K, Gheuens, J, Martin, J J, Vandenberghe, A, Van Broeckhoven, C
Publicado em 1990