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C Goizet

Showing results (11-20 of 49) with videos related to

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Acta Paediatrica (Oslo, Norway : 1992)|September 24, 2004
Phenotypic heterogeneity in AAAS gene mutationP Barat, C Goizet, A Tullio-Pelet, et al.
Revue Neurologique|June 1, 2016
Classifications of neurogenetic diseases: An increasingly complex problemJ-M Vallat, C Goizet, M Tazir, et al.
Journal of Medical Genetics|January 3, 2001
Leucodystrophy and oculocutaneous albinism in a child with an 11q14 deletionI Coupry, L Taine, C Goizet, et al.
Clinical Otolaryngology : Official Journal of ENT-UK ; Official Journal of Netherlands Society for Oto-Rhino-Laryngology & Cervico-Facial Surgery|December 30, 2016
Efficacy and safety of propranolol for epistaxis in hereditary haemorrhagic telangiectasia: retrospective, then prospective study, in a total of 21 patientsA Contis, N Gensous, J F Viallard, et al.
The British Journal of Dermatology|August 10, 2005
Hereditary mucoepithelial dysplasia: clinical, ultrastructural and genetic study of eight patients and literature reviewF Boralevi, M Haftek, P Vabres, et al.
European Journal of Medical Genetics|November 30, 2019
Severe Thoracic and Spinal Bone Abnormalities in neurofibromatosis type 1L Prudhomme, C Delleci, A Trimouille, et al.
Annales De Genetique|January 1, 1997
18p monosomy with midline defects and a de novo satellite identified by FISHL Taine, C Goizet, Z Q Wen, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|September 8, 2004
[A tumour of the right forefinger]C Espil-Taris, C Goizet, S Ramirez Del Villar, et al.
Neurology|December 10, 2008
Stroke following pulmonary arteriovenous fistula embolization in a patient with HHTS Felix, S Jeannin, C Goizet, et al.
Neuropediatrics|July 4, 2007
Bardet-biedl syndrome and brain abnormalitiesC Rooryck, S Pelras, J-F Chateil, et al.
Pageof 5

Showing results (11-20 of 49) with videos related to

Sort By:
Pageof 5
Acta Paediatrica (Oslo, Norway : 1992)|September 24, 2004
Phenotypic heterogeneity in AAAS gene mutationP Barat, C Goizet, A Tullio-Pelet, et al.
Revue Neurologique|June 1, 2016
Classifications of neurogenetic diseases: An increasingly complex problemJ-M Vallat, C Goizet, M Tazir, et al.
Journal of Medical Genetics|January 3, 2001
Leucodystrophy and oculocutaneous albinism in a child with an 11q14 deletionI Coupry, L Taine, C Goizet, et al.
Clinical Otolaryngology : Official Journal of ENT-UK ; Official Journal of Netherlands Society for Oto-Rhino-Laryngology & Cervico-Facial Surgery|December 30, 2016
Efficacy and safety of propranolol for epistaxis in hereditary haemorrhagic telangiectasia: retrospective, then prospective study, in a total of 21 patientsA Contis, N Gensous, J F Viallard, et al.
The British Journal of Dermatology|August 10, 2005
Hereditary mucoepithelial dysplasia: clinical, ultrastructural and genetic study of eight patients and literature reviewF Boralevi, M Haftek, P Vabres, et al.
European Journal of Medical Genetics|November 30, 2019
Severe Thoracic and Spinal Bone Abnormalities in neurofibromatosis type 1L Prudhomme, C Delleci, A Trimouille, et al.
Annales De Genetique|January 1, 1997
18p monosomy with midline defects and a de novo satellite identified by FISHL Taine, C Goizet, Z Q Wen, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|September 8, 2004
[A tumour of the right forefinger]C Espil-Taris, C Goizet, S Ramirez Del Villar, et al.
Neurology|December 10, 2008
Stroke following pulmonary arteriovenous fistula embolization in a patient with HHTS Felix, S Jeannin, C Goizet, et al.
Neuropediatrics|July 4, 2007
Bardet-biedl syndrome and brain abnormalitiesC Rooryck, S Pelras, J-F Chateil, et al.
Pageof 5