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F M Meire

Showing results (11-20 of 27) with videos related to

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Bulletin De La Societe Belge D'Ophtalmologie|January 1, 1992
Congenital Marfan syndrome with contractures. A clinicopathological reportF M Meire, J Van Egmond, M Hanssens
The British Journal of Ophthalmology|February 24, 2001
Use of mitomycin C and r-tPA for the management of conjunctival membrane and cataracts in a child with conjunctivitis lignosaF M Meire, I Claerhout, P H Kestelyn
Ophthalmic Genetics|February 11, 1998
Microcephaly with chorioretinopathy. A report of two dominant families and three sporadic casesM M van Genderen, J Schuil, F M Meire
Ophthalmic Genetics|January 23, 1999
Isolated Norrie disease in a female caused by a balanced translocation t(X,6)F M Meire, B A Lafaut, F Speleman, et al.
Ophthalmic Paediatrics and Genetics|March 1, 1991
Ocular manifestations of congenital Marfan syndrome with contractures (CMC syndrome)F M Meire, W J Delleman, E M Bleeker-Wagemakers
Bulletin De La Societe Belge D'Ophtalmologie|November 13, 2001
Ophthalmologic and systemic features of the Alström syndrome: report of 9 casesK Van den Abeele, M Craen, J Schuil, et al.
Human Genetics|June 1, 1991
A third allele of the PstI RFLP at DXS94M Oehler, E Schwinger, F M Meire, 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.
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.
Pageof 3

Showing results (11-20 of 27) with videos related to

Sort By:
Pageof 3
Bulletin De La Societe Belge D'Ophtalmologie|January 1, 1992
Congenital Marfan syndrome with contractures. A clinicopathological reportF M Meire, J Van Egmond, M Hanssens
The British Journal of Ophthalmology|February 24, 2001
Use of mitomycin C and r-tPA for the management of conjunctival membrane and cataracts in a child with conjunctivitis lignosaF M Meire, I Claerhout, P H Kestelyn
Ophthalmic Genetics|February 11, 1998
Microcephaly with chorioretinopathy. A report of two dominant families and three sporadic casesM M van Genderen, J Schuil, F M Meire
Ophthalmic Genetics|January 23, 1999
Isolated Norrie disease in a female caused by a balanced translocation t(X,6)F M Meire, B A Lafaut, F Speleman, et al.
Ophthalmic Paediatrics and Genetics|March 1, 1991
Ocular manifestations of congenital Marfan syndrome with contractures (CMC syndrome)F M Meire, W J Delleman, E M Bleeker-Wagemakers
Bulletin De La Societe Belge D'Ophtalmologie|November 13, 2001
Ophthalmologic and systemic features of the Alström syndrome: report of 9 casesK Van den Abeele, M Craen, J Schuil, et al.
Human Genetics|June 1, 1991
A third allele of the PstI RFLP at DXS94M Oehler, E Schwinger, F M Meire, 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.
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.
Pageof 3