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European Journal of Pediatrics|June 1, 1996
Nemaline myopathy in the neonate: two case reportsF Vendittelli, C Manciet-Labarchède, B Gilbert-DussardierJournal Francais D'Ophtalmologie|February 9, 2007
[Oguchi disease or stationary congenital night blindness: a case report]M Boissonnot, M F Robert, B Gilbert-Dussardier, et al.Rhinology|July 12, 2011
Altered quality of life in Rendu-Osler-Weber disease related to recurrent epistaxisI Ingrand, P Ingrand, B Gilbert-Dussardier, et al.Gynecologie, Obstetrique & Fertilite|July 4, 2009
[Molecular biology usefulness for rapid diagnosis of Down's syndrome and common aneuploidies]A-L Fauret, F Bilan, S Patri, et al.Rhinology|June 26, 2008
Nasal polyposis: is there an inheritance pattern? A single family studyA Delagrand, B Gilbert-Dussardier, S Burg, et al.Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|December 23, 2008
[Williams-Beuren syndrome: a multidisciplinary approach]A Lacroix, M Pezet, A Capel, et al.Neurogenetics|October 20, 2005
Screening of ARX in mental retardation families: Consequences for the strategy of molecular diagnosisK Poirier, D Lacombe, B Gilbert-Dussardier, et al.Clinical Genetics|June 25, 2013
Split hand/foot malformation with long-bone deficiency and BHLHA9 duplication: report of 13 new familiesF Petit, A-S Jourdain, J Andrieux, et al.Neuromuscular Disorders : NMD|July 6, 2011
Intragenic rearrangements in LARGE and POMGNT1 genes in severe dystroglycanopathiesS Vuillaumier-Barrot, C Bouchet-Seraphin, M Chelbi, et al.Oncogene|January 29, 2014
SPRED1, a RAS MAPK pathway inhibitor that causes Legius syndrome, is a tumour suppressor downregulated in paediatric acute myeloblastic leukaemiaE Pasmant, B Gilbert-Dussardier, A Petit, et al.Pageof 2