An explanation for the constitutive exon 9 cassette splicing of the DMD geneREISS, J; RININSLAND, F.Human molecular genetics (Print). 1994, Vol 3, Num 2, pp 295-298, issn 0964-6906Article

Microlesions and polymorphisms in the Duchenne/Becker muscular dystrophy geneRININSLAND, F; REISS, J.Human genetics. 1994, Vol 94, Num 2, pp 111-116, issn 0340-6717Article

Simple non-radioactive detection of the CFTR mutation N1303K by artificial creation of a restriction siteBAL, J; RININSLAND, F; OSBORNE, L et al.Molecular and cellular probes. 1992, Vol 6, Num 1, pp 9-11, issn 0890-8508Article

Skipping of multiple CFTR exons is not a result of single exon omissionsRICKERS, A; RININSLAND, F; OSBORNE, L et al.Human genetics. 1994, Vol 94, Num 3, pp 311-313, issn 0340-6717Article

Identification of a new DMD gene deletion by ectopic transcript analysisRININSLAND, F; HAHN, A; NIEMANN-SEYDE, S et al.Journal of medical genetics. 1992, Vol 29, Num 9, pp 647-651, issn 0022-2593Article

A comprehensive CFTR mutation analysis of German cystic fibrosis patientsREISS, J; ELLERMEYER, U; RININSLAND, F et al.Human molecular genetics (Print). 1993, Vol 2, Num 6, pp 809-811, issn 0964-6906Article

Single-strand conformation polymorphism (SSCP) analysis of exon 11 of the CFTR gene reliably detects more than one third of non-ΔF508 mutations in German cystic fibrosis patientsPLIETH, J; RININSLAND, F; SCHLÖSSER, M et al.Human genetics. 1992, Vol 88, Num 3, pp 283-287, issn 0340-6717Article

A novel CFTR mutation, 4035delA, detected by non-radioactive SSCP analysisREISS, J; LENZ, U; RININSLAND, F et al.Human genetics. 1992, Vol 90, Num 3, pp 303-304, issn 0340-6717Article

Granzyme B ELISPOT assay for ex vivo measurements of T cell immunityRININSLAND, F. H; HELMS, T; ASAAD, R. J et al.Journal of immunological methods. 2000, Vol 240, Num 1-2, pp 143-155, issn 0022-1759Article