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Showing results (311-320 of 488) with videos related to

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Acta Cytologica|December 9, 1997
Pulmonary malakoplakia diagnosed by fine needle aspiration. A case reportC Lambert, T Gansler, K A Mansour, et al.
The Journal of General Virology|July 1, 1997
A cDNA clone from a defective RNA of citrus tristeza virus is infective in the presence of the helper virusG Yang, M Mawassi, L Ashoulin, et al.
Ophthalmic Paediatrics and Genetics|December 1, 1990
Posthumous diagnosis of X-linked retinoschisis using DNA analysisM J van Schooneveld, E M Bleeker-Wagemakers, U Orth, et al.
Chest|October 16, 2002
Saprophytic fungal infections and complications involving the bronchial anastomosis following human lung transplantationDavid R Nunley, Anthony A Gal, J David Vega, et al.
Investigative Ophthalmology & Visual Science|August 11, 2000
Early-onset severe rod-cone dystrophy in young children with RPE65 mutationsB Lorenz, P Gyürüs, M Preising, et al.
Human Molecular Genetics|July 1, 1994
Three novel rhodopsin mutations (C110F, L131P, A164V) in patients with autosomal dominant retinitis pigmentosaS Fuchs, H Kranich, M J Denton, et al.
Neuroscience|April 20, 2005
Mild Pelizaeus-Merzbacher disease caused by a point mutation affecting correct splicing of PLP1 mRNAC A Hübner, A Senning, U Orth, et al.
Human Molecular Genetics|December 1, 1993
Heterozygous 'null allele' mutation in the human peripherin/RDS geneM Meins, G Grüning, A Blankenagel, et al.
Human Molecular Genetics|January 1, 1996
Autosomal recessive non-syndromic deafness locus (DFNB8) maps on chromosome 21q22 in a large consanguineous kindred from PakistanA Veske, R Oehlmann, F Younus, et al.
Human Molecular Genetics|April 1, 1994
A missense point mutation (Leu13Arg) of the Norrie disease gene in a large Cuban kindred with Norrie diseaseS Fuchs, S Y Xu, M Caballero, et al.
Pageof 49

Showing results (311-320 of 488) with videos related to

Sort By:
Pageof 49
Acta Cytologica|December 9, 1997
Pulmonary malakoplakia diagnosed by fine needle aspiration. A case reportC Lambert, T Gansler, K A Mansour, et al.
The Journal of General Virology|July 1, 1997
A cDNA clone from a defective RNA of citrus tristeza virus is infective in the presence of the helper virusG Yang, M Mawassi, L Ashoulin, et al.
Ophthalmic Paediatrics and Genetics|December 1, 1990
Posthumous diagnosis of X-linked retinoschisis using DNA analysisM J van Schooneveld, E M Bleeker-Wagemakers, U Orth, et al.
Chest|October 16, 2002
Saprophytic fungal infections and complications involving the bronchial anastomosis following human lung transplantationDavid R Nunley, Anthony A Gal, J David Vega, et al.
Investigative Ophthalmology & Visual Science|August 11, 2000
Early-onset severe rod-cone dystrophy in young children with RPE65 mutationsB Lorenz, P Gyürüs, M Preising, et al.
Human Molecular Genetics|July 1, 1994
Three novel rhodopsin mutations (C110F, L131P, A164V) in patients with autosomal dominant retinitis pigmentosaS Fuchs, H Kranich, M J Denton, et al.
Neuroscience|April 20, 2005
Mild Pelizaeus-Merzbacher disease caused by a point mutation affecting correct splicing of PLP1 mRNAC A Hübner, A Senning, U Orth, et al.
Human Molecular Genetics|December 1, 1993
Heterozygous 'null allele' mutation in the human peripherin/RDS geneM Meins, G Grüning, A Blankenagel, et al.
Human Molecular Genetics|January 1, 1996
Autosomal recessive non-syndromic deafness locus (DFNB8) maps on chromosome 21q22 in a large consanguineous kindred from PakistanA Veske, R Oehlmann, F Younus, et al.
Human Molecular Genetics|April 1, 1994
A missense point mutation (Leu13Arg) of the Norrie disease gene in a large Cuban kindred with Norrie diseaseS Fuchs, S Y Xu, M Caballero, et al.
Pageof 49