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H Dollfus

Showing results (21-30 of 72) with videos related to

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Annales De Genetique|February 16, 2000
Schinzel-Giedion syndrome with severe deafness and neurodegenerative processY Alembik, D Christmann, A de Saint Martin, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 8, 2006
Myopathy with tubular aggregates and gyrate atrophy of the choroid and retina due to hyperornithinaemiaM Fleury, R Barbier, F Ziegler, et al.
Journal of Neuro-Ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society|September 26, 1997
Unusual scotomas after transsphenoidal surgery of a pituitary macroadenomaH Dollfus, S Gomberg, P Touraine, et al.
Journal of Medical Genetics|July 28, 2001
Identification of a new TWIST mutation (7p21) with variable eyelid manifestations supports locus homogeneity of BPES at 3q22H Dollfus, G Kumaramanickavel, P Biswas, et al.
Human Genetics|June 1, 1996
Evidence of genetic heterogeneity of Leber's congenital amaurosis (LCA) and mapping of LCA1 to chromosome 17p13A Camuzat, J M Rozet, H Dollfus, et al.
European Journal of Neurology|November 23, 2006
Late onset stroke and myocardial infarction in Williams syndromeF Blanc, V Wolff, V Talmant, et al.
Journal Francais D'Ophtalmologie|March 16, 2005
[Update on Bardet-Biedl syndrome]H Dollfus, A Verloes, D Bonneau, et al.
Clinical Genetics|November 21, 2015
Value of MRI olfactory bulb evaluation in the assessment of olfactory dysfunction in Bardet-Biedl syndromeJ J Braun, V Noblet, S Kremer, et al.
Journal Francais D'Ophtalmologie|June 12, 2009
[Epidemiology of age related macular degeneration]N Leveziel, C Delcourt, J Zerbib, et al.
Clinical Genetics|January 10, 2014
Mutation spectrum in BBS genes guided by homozygosity mapping in an Indian cohortC Sathya Priya, P Sen, V Umashankar, et al.
Pageof 8

Showing results (21-30 of 72) with videos related to

Sort By:
Pageof 8
Annales De Genetique|February 16, 2000
Schinzel-Giedion syndrome with severe deafness and neurodegenerative processY Alembik, D Christmann, A de Saint Martin, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 8, 2006
Myopathy with tubular aggregates and gyrate atrophy of the choroid and retina due to hyperornithinaemiaM Fleury, R Barbier, F Ziegler, et al.
Journal of Neuro-Ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society|September 26, 1997
Unusual scotomas after transsphenoidal surgery of a pituitary macroadenomaH Dollfus, S Gomberg, P Touraine, et al.
Journal of Medical Genetics|July 28, 2001
Identification of a new TWIST mutation (7p21) with variable eyelid manifestations supports locus homogeneity of BPES at 3q22H Dollfus, G Kumaramanickavel, P Biswas, et al.
Human Genetics|June 1, 1996
Evidence of genetic heterogeneity of Leber's congenital amaurosis (LCA) and mapping of LCA1 to chromosome 17p13A Camuzat, J M Rozet, H Dollfus, et al.
European Journal of Neurology|November 23, 2006
Late onset stroke and myocardial infarction in Williams syndromeF Blanc, V Wolff, V Talmant, et al.
Journal Francais D'Ophtalmologie|March 16, 2005
[Update on Bardet-Biedl syndrome]H Dollfus, A Verloes, D Bonneau, et al.
Clinical Genetics|November 21, 2015
Value of MRI olfactory bulb evaluation in the assessment of olfactory dysfunction in Bardet-Biedl syndromeJ J Braun, V Noblet, S Kremer, et al.
Journal Francais D'Ophtalmologie|June 12, 2009
[Epidemiology of age related macular degeneration]N Leveziel, C Delcourt, J Zerbib, et al.
Clinical Genetics|January 10, 2014
Mutation spectrum in BBS genes guided by homozygosity mapping in an Indian cohortC Sathya Priya, P Sen, V Umashankar, et al.
Pageof 8