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A Gal

Showing results (341-350 of 488) with videos related to

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Nature Genetics|September 1, 1994
Missense rhodopsin mutation in a family with recessive RPG Kumaramanickavel, M Maw, M J Denton, et al.
Human Genetics|September 1, 1993
Molecular analysis in patients with mucopolysaccharidosis type II suggests that DXS466 maps within the Hunter geneC Steglich, S Bunge, T Hulsebos, et al.
Domestic Animal Endocrinology|October 5, 2019
The effect of the sodium-glucose cotransporter type-2 inhibitor dapagliflozin on glomerular filtration rate in healthy catsA Gal, S E Burton, K Weidgraaf, et al.
Human Mutation|March 27, 1999
Twelve novel myosin VIIA mutations in 34 patients with Usher syndrome type I: confirmation of genetic heterogeneityA R Janecke, M Meins, M Sadeghi, et al.
Human Genetics|June 1, 1986
Choroideremia-locus maps between DXS3 and DXS11 on XqA Gal, F Brunsmann, D Hogenkamp, et al.
Fortschritte Der Ophthalmologie : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|January 1, 1991
[Autosomal dominant hereditary retinopathia pigmentosa with genetic heterogeneity]U Orth, C Samanns, H Gusseck, et al.
Chest|February 7, 2001
The surgical spectrum of pulmonary neuroendocrine neoplasmsW A Cooper, V H Thourani, A A Gal, et al.
Journal of Medical Genetics|May 1, 1995
Oguchi disease: suggestion of linkage to markers on chromosome 2qM A Maw, S John, S Jablonka, et al.
Genomics|March 15, 1994
Mapping of the autosomal dominant exudative vitreoretinopathy locus (EVR1) by multipoint linkage analysis in four familiesB Müller, U Orth, C E van Nouhuys, et al.
Human Molecular Genetics|November 1, 1994
Three sequence polymorphisms in the PDC geneF C Mansergh, S A Jordan, G J Farrar, et al.
Pageof 49

Showing results (341-350 of 488) with videos related to

Sort By:
Pageof 49
Nature Genetics|September 1, 1994
Missense rhodopsin mutation in a family with recessive RPG Kumaramanickavel, M Maw, M J Denton, et al.
Human Genetics|September 1, 1993
Molecular analysis in patients with mucopolysaccharidosis type II suggests that DXS466 maps within the Hunter geneC Steglich, S Bunge, T Hulsebos, et al.
Domestic Animal Endocrinology|October 5, 2019
The effect of the sodium-glucose cotransporter type-2 inhibitor dapagliflozin on glomerular filtration rate in healthy catsA Gal, S E Burton, K Weidgraaf, et al.
Human Mutation|March 27, 1999
Twelve novel myosin VIIA mutations in 34 patients with Usher syndrome type I: confirmation of genetic heterogeneityA R Janecke, M Meins, M Sadeghi, et al.
Human Genetics|June 1, 1986
Choroideremia-locus maps between DXS3 and DXS11 on XqA Gal, F Brunsmann, D Hogenkamp, et al.
Fortschritte Der Ophthalmologie : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|January 1, 1991
[Autosomal dominant hereditary retinopathia pigmentosa with genetic heterogeneity]U Orth, C Samanns, H Gusseck, et al.
Chest|February 7, 2001
The surgical spectrum of pulmonary neuroendocrine neoplasmsW A Cooper, V H Thourani, A A Gal, et al.
Journal of Medical Genetics|May 1, 1995
Oguchi disease: suggestion of linkage to markers on chromosome 2qM A Maw, S John, S Jablonka, et al.
Genomics|March 15, 1994
Mapping of the autosomal dominant exudative vitreoretinopathy locus (EVR1) by multipoint linkage analysis in four familiesB Müller, U Orth, C E van Nouhuys, et al.
Human Molecular Genetics|November 1, 1994
Three sequence polymorphisms in the PDC geneF C Mansergh, S A Jordan, G J Farrar, et al.
Pageof 49