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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.
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.
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