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Genetic Testing|September 12, 2001
Carrier screening for cystic fibrosis in a prenatal settingI Delvaux, A van Tongerloo, L Messiaen, et al.Human Reproduction (Oxford, England)|April 29, 1998
Fluorescent in-situ hybridization on human embryos showing cleavage arrest after freezing and thawingH Laverge, J Van der Elst, P De Sutter, et al.Human Genetics|March 1, 1988
Linkage of a polymorphic marker for the type III collagen gene (COL3A1) to atypical autosomal dominant Ehlers-Danlos syndrome type IV in a large Belgian pedigreeA C Nicholls, A De Paepe, P Narcisi, et al.Human Mutation|July 9, 2004
Comprehensive molecular screening of the FBN1 gene favors locus homogeneity of classical Marfan syndromeB Loeys, J De Backer, P Van Acker, et al.Cancer Genetics and Cytogenetics|September 1, 1997
Comparative genomic hybridization analysis of human neuroblastomas: detection of distal 1p deletions and further molecular genetic characterization of neuroblastoma cell linesN Van Roy, A Jauch, M Van Gele, et al.Genes, Chromosomes & Cancer|July 1, 1997
Monosomy 22 in a mixed germ cell-sex cord-stromal tumor of the ovaryF Speleman, B Dermaut, C R De Potter, et al.Cell Biochemistry and Function|June 1, 1996
Proteoglycan alterations in skin fibroblast cultures from patients affected with pseudoxanthoma elasticumA Passi, R Albertini, M Baccarani Contri, et al.Nature Genetics|June 1, 1992
Evidence for a relationship between Ehlers-Danlos type VII C in humans and bovine dermatosparaxisB V Nusgens, C Verellen-Dumoulin, T Hermanns-Lê, et al.Medical and Pediatric Oncology|December 7, 2000
Chromosome 2 short arm translocations revealed by M-FISH analysis of neuroblastoma cell linesN Van Roy, H Van Limbergen, J Vandesompele, et al.The British Journal of Dermatology|July 1, 1987
Ehlers-Danlos syndrome type I: a clinical and ultrastructural study of a family with reduced amounts of collagen type IIIA De Paepe, A Nicholls, P Narcisi, et al.Pageof 15