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Human Mutation|January 1, 1994
Mutation detection by denaturing gradient gel electrophoresis (DGGE)R Fodde, M LosekootEndocrine Development|November 28, 2012
Spectrum of insulin-like growth factor deficiencyJan M Wit, W Oostdijk, M LosekootNederlands Tijdschrift Voor Geneeskunde|June 21, 2001
[From gene to disease; achondroplasia and other skeletal dysplasias due to an activating mutation in the fibroblast growth factor]C M van Ravenswaaij-Arts, M LosekootNederlands Tijdschrift Voor Geneeskunde|August 4, 2001
[From gene to disease; 'maturity-onset diabetes of the young' (MODY), monogenetic inheritable forms of diabetes mellitus]J A Maassen, H H Lemkes, M LosekootNederlands Tijdschrift Voor Geneeskunde|November 29, 2001
[From gene to disease; HD gene and Huntington disease]J A Maat-Kievit, M Losekoot, R A RoosEndocrine Development|February 9, 2013
Molecular IGF-1 and IGF-1 receptor defects: from genetics to clinical managementM J E Walenkamp, M Losekoot, J M WitGenomics|December 1, 1990
Nucleotide sequence of the Belgian G gamma+(A gamma delta beta)0-thalassemia deletion breakpoint suggests a common mechanism for a number of such recombination eventsR Fodde, M Losekoot, L Casula, et al.Human Genetics|August 1, 1989
A novel delta zero-thalassemia arising from a frameshift insertion, detected by direct sequencing of enzymatically amplified DNAM Losekoot, R Fodde, P C Giordano, et al.European Journal of Human Genetics : EJHG|April 10, 1999
A European pilot quality assessment scheme for molecular diagnosis of Huntington's diseaseM Losekoot, B Bakker, F Laccone, et al.Oncogene|May 1, 1987
Novel transforming sequences in human acute myelocytic leukemia cell linesJ W Janssen, A C Steenvoorden, M Losekoot, et al.Pageof 7