Showing results (171-180 of 271) with videos related to
Sort By:
Pageof 28
Genetic Counseling (Geneva, Switzerland)|November 5, 1999
A novel 7.4 kb mitochondrial deletion in a patient with congenital progressive external ophthalmoplegia, muscle weakness and mental retardationM Tabaku, E Legius, W Robberecht, et al.Journal of Medical Genetics|April 1, 1997
Prader-Willi syndrome in a child with mosaic trisomy 15 and mosaic triplo-X: a molecular analysisK Devriendt, G Matthijs, S Claes, et al.Annales De Genetique|January 1, 1997
Agenesis of corpus callosum and anophthalmia in the asplenia syndrome. A recognisable association?K Devriendt, G Naulaers, G Matthijs, et al.Biomaterials|March 29, 2000
Characterization of protein-resistant dextran monolayersR A Frazie, G Matthijs, M C Davies, et al.Blood|March 7, 1998
Fluorescence in situ hybridization characterization of new translocations involving TEL (ETV6) in a wide spectrum of hematologic malignanciesI Wlodarska, R La Starza, M Baens, et al.Human Genetics|September 1, 1990
Association between XV2c/CS7/KM19/D9 haplotypes and the delta F508 mutation. A study of 57 Belgian familiesH Cuppens, E Legius, P Cabello, et al.Blood|March 9, 2000
Inv(2)(p23q35) in anaplastic large-cell lymphoma induces constitutive anaplastic lymphoma kinase (ALK) tyrosine kinase activation by fusion to ATIC, an enzyme involved in purine nucleotide biosynthesisZ Ma, J Cools, P Marynen, et al.Journal of Medical Genetics|February 1, 2008
Deletion of C2orf34, PREPL and SLC3A1 causes atypical hypotonia-cystinuria syndromeB Chabrol, K Martens, S Meulemans, et al.Journal of Vascular Surgery Cases and Innovative Techniques|August 21, 2025
Percutaneous transthoracic coil embolization of a gutter-related type Ia endoleak after chimney thoracic endovascular aortic repairEmiel W M Huistra, Ignace F J Tielliu, Aryan Mazuri, et al.BMJ Case Reports|June 21, 2011
Deletion of C2orf34, PREPL and SLC3A1 causes atypical hypotonia-cystinuria syndromeB Chabrol, K Martens, S Meulemans, et al.Pageof 28