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American Journal of Human Genetics|March 1, 1994
Identification of internal variation in the pseudoautosomal VNTR DXYS17, with nonrandom distribution of the alleles on the X and the Y chromosomesR Decorte, R Wu, P Marynen, et al.Annual Review of Genomics and Human Genetics|November 10, 2001
Congenital disorders of glycosylationJ Jaeken, G MatthijsAnnals of Oncology : Official Journal of the European Society for Medical Oncology|July 25, 2000
The product of the t(11;18), an API2-MLT fusion, is an almost exclusive finding in marginal zone cell lymphoma of extranodal MALT-typeB Maes, M Baens, P Marynen, et al.Genomics|July 20, 1995
Identification of a novel conserved human gene, TEGTL Walter, P Marynen, J Szpirer, et al.Human Genetics|July 8, 1998
Structural organisation of the gene encoding the alpha-subunit of the human amiloride-sensitive epithelial sodium channelM Ludwig, U Bolkenius, L Wickert, et al.FEMS Microbiology Letters|November 15, 1992
Detection of bacterial and mycoplasma contamination in cell cultures by polymerase chain reactionM Spaepen, A F Angulo, P Marynen, et al.Genomics|December 1, 1993
Detection of 98.5% of the mutations in 200 Belgian cystic fibrosis alleles by reverse dot-blot and sequencing of the complete coding region and exon/intron junctions of the CFTR geneH Cuppens, P Marynen, C De Boeck, et al.Genome Research|May 1, 1996
Genomic organization of TEL: the human ETS-variant gene 6M Baens, P Peeters, C Guo, et al.Leukemia|August 1, 1997
A new breakpoint, telomeric to TEL/ETV6, on the short arm of chromosome 12 in T cell acute lymphoblastic leukemiaM Le Coniat, V Della Valle, P Marynen, et al.American Journal of Human Genetics|April 25, 2000
Unequal meiotic crossover: a frequent cause of NF1 microdeletionsC López Correa, H Brems, C Lázaro, et al.Pageof 28