Citation: Jcfm. Dreesen et al., Multiplex PCR of polymorphic markers flanking the CFTR gene; a general approach for preimplantation genetic diagnosis of cystic fibrosis, MOL HUM REP, 6(5), 2000, pp. 391-396
Authors:
Jongbloed, RJE
Wilde, AAM
Geelen, JLMC
Doevendans, F
Schaap, C
Van Langen, I
van Tintelen, JP
Cobben, JM
Beaufort-Krol, GCM
Geraedts, JPM
Smeets, HJM
Citation: Rje. Jongbloed et al., Novel KCNQ1 and HERG missense mutations in Dutch long-QT families (vol 13,pg 301, 1998), HUM MUTAT, 14(1), 1999, pp. 86-86
Authors:
Jongbloed, RJE
Wilde, AAM
Geelen, JLMC
Doevendans, P
Schaap, C
Van Langen, I
van Tintelen, JP
Cobben, JM
Beaufort-Krol, GCM
Geraedts, JPM
Smeets, HJM
Citation: Rje. Jongbloed et al., Novel KCNQ1 and HERG missense mutations in Dutch long-QT families, HUM MUTAT, 13(4), 1999, pp. 301-310
Authors:
de Coo, RFM
Buddiger, PAL
Smeets, HJM
van Oost, BA
Citation: Rfm. De Coo et al., The structure of the human NDUFV1 gene encoding the 51-kDa subunit of mitochondrial complex I, MAMM GENOME, 10(1), 1999, pp. 49-53
Authors:
Wilde, AAM
Jongbloed, RJE
Doevendans, PA
Duren, DR
Hauer, RNW
van Langen, IM
van Tintelen, JP
Smeets, HJM
Meyer, H
Geelen, JLMC
Citation: Aam. Wilde et al., Auditory stimuli as a trigger for arrhythmic events differentiate HERG-related (LQTS(2)) patients from KVLQT1-related patients (LQTS(1)), J AM COL C, 33(2), 1999, pp. 327-332
Authors:
De Coo, IFM
Renier, WO
Ruitenbeek, W
Ter Laak, HJ
Bakker, M
Schagger, H
Van Oost, BA
Smeets, HJM
Citation: Ifm. De Coo et al., A 4-base pair deletion in the mitochondrial cytochrome b gene associated with parkinsonism/MELAS overlap syndrome, ANN NEUROL, 45(1), 1999, pp. 130-133
Authors:
Van der Loop, FTL
Monnens, LAH
Schroder, CH
Lemmink, HH
Breuning, MH
Timmer, EDJ
Smeets, HJM
Citation: Ftl. Van Der Loop et al., Identification of COL4 A5 defects in Alport's syndrome by immunohistochemistry of skin (vol 55, pg 1217, 1999), KIDNEY INT, 56(6), 1999, pp. 2337-2337
Authors:
van der Loop, FTL
Monnens, LAH
Schroder, CH
Lemmink, HH
Breuning, MH
Timmer, EDJ
Smeets, HJM
Citation: Ftl. Van Der Loop et al., Identification of COL4A5 defects in Alport's syndrome by immunohistochemistry of skin, KIDNEY INT, 55(4), 1999, pp. 1217-1224