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F Meire

Showing results (41-50 of 54) with videos related to

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Archives of Neurology|August 2, 2001
A new mitochondrial point mutation in the transfer RNA(Leu) gene in a patient with a clinical phenotype resembling Kearns-Sayre syndromeS Seneca, H Verhelst, L De Meirleir, et al.
Genomics|November 1, 1993
Additional evidence for a gene locus for progressive cone dystrophy with late rod involvement in Xp21.1-p11.3A A Bergen, F Meire, J ten Brink, et al.
Genomics|September 20, 1995
Gene conversion between red and defective green opsin gene in blue cone monochromacyE Reyniers, M N Van Thienen, F Meire, et al.
Journal of Medical Genetics|October 1, 1996
Conclusive evidence for a distinct congenital stationary night blindness locus in Xp21.1A A Bergen, J B ten Brink, F Riemslag, et al.
The British Journal of Ophthalmology|June 30, 2000
Sorsby fundus dystrophy without a mutation in the TIMP-3 geneJ J Assink, E de Backer, J B ten Brink, et al.
American Journal of Medical Genetics|April 15, 1993
Heterogeneity versus variability in megalocornea-mental retardation (MMR) syndromes: report of new cases and delineation of 4 probable typesA Verloes, H Journel, C Elmer, et al.
American Journal of Human Genetics|November 1, 1994
Features of mtDNA mutation patterns in European pedigrees and sporadic cases with Leber hereditary optic neuropathyB Obermaier-Kusser, B Lorenz, S Schubring, et al.
Journal of Computer Assisted Tomography|July 27, 2001
Imaging studies in the diagnostic workup of neonatal nasal obstructionB D Vanzieleghem, M M Lemmerling, H F Vermeersch, et al.
Thrombosis and Haemostasis|July 4, 2001
Homozygous and compound-heterozygous type I plasminogen deficiency is a common cause of ligneous conjunctivitisV Schuster, P Zeitler, S Seregard, et al.
Cancer Genetics and Cytogenetics|October 15, 1994
Chromosome aberrations in fibrous dysplasiaP Dal Cin, R Sciot, F Speleman, et al.
Pageof 6

Showing results (41-50 of 54) with videos related to

Sort By:
Pageof 6
Archives of Neurology|August 2, 2001
A new mitochondrial point mutation in the transfer RNA(Leu) gene in a patient with a clinical phenotype resembling Kearns-Sayre syndromeS Seneca, H Verhelst, L De Meirleir, et al.
Genomics|November 1, 1993
Additional evidence for a gene locus for progressive cone dystrophy with late rod involvement in Xp21.1-p11.3A A Bergen, F Meire, J ten Brink, et al.
Genomics|September 20, 1995
Gene conversion between red and defective green opsin gene in blue cone monochromacyE Reyniers, M N Van Thienen, F Meire, et al.
Journal of Medical Genetics|October 1, 1996
Conclusive evidence for a distinct congenital stationary night blindness locus in Xp21.1A A Bergen, J B ten Brink, F Riemslag, et al.
The British Journal of Ophthalmology|June 30, 2000
Sorsby fundus dystrophy without a mutation in the TIMP-3 geneJ J Assink, E de Backer, J B ten Brink, et al.
American Journal of Medical Genetics|April 15, 1993
Heterogeneity versus variability in megalocornea-mental retardation (MMR) syndromes: report of new cases and delineation of 4 probable typesA Verloes, H Journel, C Elmer, et al.
American Journal of Human Genetics|November 1, 1994
Features of mtDNA mutation patterns in European pedigrees and sporadic cases with Leber hereditary optic neuropathyB Obermaier-Kusser, B Lorenz, S Schubring, et al.
Journal of Computer Assisted Tomography|July 27, 2001
Imaging studies in the diagnostic workup of neonatal nasal obstructionB D Vanzieleghem, M M Lemmerling, H F Vermeersch, et al.
Thrombosis and Haemostasis|July 4, 2001
Homozygous and compound-heterozygous type I plasminogen deficiency is a common cause of ligneous conjunctivitisV Schuster, P Zeitler, S Seregard, et al.
Cancer Genetics and Cytogenetics|October 15, 1994
Chromosome aberrations in fibrous dysplasiaP Dal Cin, R Sciot, F Speleman, et al.
Pageof 6