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Nederlands Tijdschrift Voor Geneeskunde|February 24, 2001
[Quality control of DNA testing in hereditary diseases]A M van den Ouweland, H SchefferNederlands Tijdschrift Voor Geneeskunde|September 4, 2001
[From gene to disease; from defective chloride ion transport to cystic fibrosis]H Scheffer, A M van den Ouweland, H J VeezeNederlands Tijdschrift Voor Geneeskunde|October 26, 2001
[From gene to disease; TSC1 and TSC2 genes and tuberous sclerosis complex]S Verhoef, D Lindhout, D J Halley, et al.Human Genetics|September 1, 1992
The QM gene is X-linked and therefore not involved in suppression of tumorigenesis in Wilms' tumorA M van den Ouweland, M Verdijk, M M Mannens, et al.Histochemistry and Cell Biology|June 17, 2000
Immunological detection of polycystin-1 in human kidneyJ Nauta, M A Goedbloed, A M van den Ouweland, et al.Biochimica Et Biophysica Acta|February 20, 1985
Characterization of the feline c-abl proto-oncogeneJ A Schalken, A M van den Ouweland, H P Bloemers, et al.Nederlands Tijdschrift Voor Geneeskunde|September 27, 2001
[From gene to disease; neurofibromatosis type 1]A de Goede-Bolder, M H Cnossen, D Dooijes, et al.Kidney International|July 1, 1994
Inheritance of mutations in the V2 receptor gene in thirteen families with nephrogenic diabetes insipidusN V Knoers, A M van den Ouweland, M Verdijk, et al.The Journal of Craniofacial Surgery|August 7, 1998
Pfeiffer's syndrome resulting from an S351C mutation in the fibroblast growth factor receptor-2 geneI M Mathijssen, J M Vaandrager, A J Hoogeboom, et al.American Journal of Medical Genetics|April 1, 1992
Validation of linkage-based DNA-diagnosis of fragile X gene carriers with the CGG repeat probeB A van Oost, A P Smits, J C Dreesen, et al.Pageof 8