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C Goizet

Showing results (1-10 of 49) with videos related to

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American Journal of Medical Genetics|December 14, 1999
W syndrome: report of three cases and reviewC Goizet, D Bonneau, D Lacombe
Journal of Medical Genetics|July 13, 2002
Predictive testing in the context of pregnancy: experience in Huntington's disease and autosomal dominant cerebellar ataxiaG Lesca, C Goizet, A Dürr
Journal De Radiologie|March 21, 2003
[Case no 4. Intracranial hypotension syndrome]V Dousset, C Goizet, V Dousset
Neurology|November 13, 2002
Presymptomatic testing in Huntington's disease and autosomal dominant cerebellar ataxiasC Goizet, G Lesca, A Dürr, et al.
Bulletin De L'Academie Nationale De Medecine|September 16, 2000
[Williams syndrome (microdeletion 7q11.23), model of behavioral phenotype]J Battin, D Lacombe, L Taine, et al.
Revue Neurologique|April 20, 2010
[Etiological assessment of cerebral infarct in the young. Proposals from the working group of the French Neuro-vascular Society (December 2008)]F Rouanet, I Sibon, C Goizet, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|December 2, 2014
[Incontinentia pigmenti with subcortical band heterotopias]A Aoun, C Goizet, B Arveiler, et al.
Genetic Counseling (Geneva, Switzerland)|September 10, 2015
RECURRENCE OF POMPE DISEASE IN FIRST COUSINSD Lacombe, J B Thambo, M Fayon, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|November 3, 2004
[Hereditary neuralgic amyotrophy: a paediatric and familial presentation of Parsonage-Turner syndrome]M Husson, C Goizet, S Rivera, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|January 1, 1997
[Does germinal chromosomal mosaicism exist?]C Goizet, L Taine, Z Q Wen, et al.
Pageof 5

Showing results (1-10 of 49) with videos related to

Sort By:
Pageof 5
American Journal of Medical Genetics|December 14, 1999
W syndrome: report of three cases and reviewC Goizet, D Bonneau, D Lacombe
Journal of Medical Genetics|July 13, 2002
Predictive testing in the context of pregnancy: experience in Huntington's disease and autosomal dominant cerebellar ataxiaG Lesca, C Goizet, A Dürr
Journal De Radiologie|March 21, 2003
[Case no 4. Intracranial hypotension syndrome]V Dousset, C Goizet, V Dousset
Neurology|November 13, 2002
Presymptomatic testing in Huntington's disease and autosomal dominant cerebellar ataxiasC Goizet, G Lesca, A Dürr, et al.
Bulletin De L'Academie Nationale De Medecine|September 16, 2000
[Williams syndrome (microdeletion 7q11.23), model of behavioral phenotype]J Battin, D Lacombe, L Taine, et al.
Revue Neurologique|April 20, 2010
[Etiological assessment of cerebral infarct in the young. Proposals from the working group of the French Neuro-vascular Society (December 2008)]F Rouanet, I Sibon, C Goizet, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|December 2, 2014
[Incontinentia pigmenti with subcortical band heterotopias]A Aoun, C Goizet, B Arveiler, et al.
Genetic Counseling (Geneva, Switzerland)|September 10, 2015
RECURRENCE OF POMPE DISEASE IN FIRST COUSINSD Lacombe, J B Thambo, M Fayon, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|November 3, 2004
[Hereditary neuralgic amyotrophy: a paediatric and familial presentation of Parsonage-Turner syndrome]M Husson, C Goizet, S Rivera, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|January 1, 1997
[Does germinal chromosomal mosaicism exist?]C Goizet, L Taine, Z Q Wen, et al.
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