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M Meire

Showing results (21-30 of 40) with videos related to

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Human Genetics|June 1, 1991
A third allele of the PstI RFLP at DXS94M Oehler, E Schwinger, F M Meire, et al.
Revue Belge De Medecine Dentaire|August 18, 2009
[Cavity preparation using an Er:YAG laser in the adult dentition]K Delmé, M Meire, M De Bruyne, et al.
Ophthalmic Genetics|January 3, 2001
Thiamine-responsive megaloblastic anemia syndrome (TRMA) with cone-rod dystrophyF M Meire, Van Genderen MM, K Lemmens, et al.
European Journal of Ophthalmology|April 1, 1991
Retinal manifestations in fibromuscular dysplasiaF M Meire, J J De Laey, M N Van Thienen, et al.
International Endodontic Journal|November 11, 2014
Endodontic performance by Flemish dentists: have they evolved?M Neukermans, J Vanobbergen, M De Bruyne, et al.
The British Journal of Ophthalmology|February 1, 1994
X linked progressive cone dystrophy. Localisation of the gene locus to Xp21-p11.1 by linkage analysisF M Meire, A A Bergen, A De Rouck, et al.
Ophthalmic Paediatrics and Genetics|September 1, 1991
X-linked megalocornea. Ocular findings and linkage analysisF M Meire, E M Bleeker-Wagemakers, M Oehler, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|April 15, 2000
Indocyanine green angiography in Sorsby's fundus dystrophyB A Lafaut, E De Backer, T Kohno, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|February 2, 2000
Vasoproliferative retinal tumors associated with peripheral chorioretinal scars in presumed congenital toxoplasmosisB A Lafaut, F M Meire, A M Leys, et al.
Ophthalmic Genetics|September 1, 1995
Neurological disorders in members of families with Leber's hereditary optic neuropathy (LHON) caused by different mitochondrial mutationsF M Meire, R Van Coster, P Cochaux, et al.
Pageof 4

Showing results (21-30 of 40) with videos related to

Sort By:
Pageof 4
Human Genetics|June 1, 1991
A third allele of the PstI RFLP at DXS94M Oehler, E Schwinger, F M Meire, et al.
Revue Belge De Medecine Dentaire|August 18, 2009
[Cavity preparation using an Er:YAG laser in the adult dentition]K Delmé, M Meire, M De Bruyne, et al.
Ophthalmic Genetics|January 3, 2001
Thiamine-responsive megaloblastic anemia syndrome (TRMA) with cone-rod dystrophyF M Meire, Van Genderen MM, K Lemmens, et al.
European Journal of Ophthalmology|April 1, 1991
Retinal manifestations in fibromuscular dysplasiaF M Meire, J J De Laey, M N Van Thienen, et al.
International Endodontic Journal|November 11, 2014
Endodontic performance by Flemish dentists: have they evolved?M Neukermans, J Vanobbergen, M De Bruyne, et al.
The British Journal of Ophthalmology|February 1, 1994
X linked progressive cone dystrophy. Localisation of the gene locus to Xp21-p11.1 by linkage analysisF M Meire, A A Bergen, A De Rouck, et al.
Ophthalmic Paediatrics and Genetics|September 1, 1991
X-linked megalocornea. Ocular findings and linkage analysisF M Meire, E M Bleeker-Wagemakers, M Oehler, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|April 15, 2000
Indocyanine green angiography in Sorsby's fundus dystrophyB A Lafaut, E De Backer, T Kohno, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|February 2, 2000
Vasoproliferative retinal tumors associated with peripheral chorioretinal scars in presumed congenital toxoplasmosisB A Lafaut, F M Meire, A M Leys, et al.
Ophthalmic Genetics|September 1, 1995
Neurological disorders in members of families with Leber's hereditary optic neuropathy (LHON) caused by different mitochondrial mutationsF M Meire, R Van Coster, P Cochaux, et al.
Pageof 4