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U Orth

Showing results (31-40 of 40) 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.
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.
Nature Genetics|November 4, 2000
Mutations in MERTK, the human orthologue of the RCS rat retinal dystrophy gene, cause retinitis pigmentosaA Gal, Y Li, D A Thompson, et al.
Journal of Medical Genetics|February 1, 1996
Five novel mutations in the L1CAM gene in families with X linked hydrocephalusS M Gu, U Orth, A Veske, et al.
Clinical Genetics|March 22, 2001
Brachytelephalangic dwarfism due to the loss of ARSE and SHOX genes resulting from an X;Y translocationJ Seidel, S Schiller, C Kelbova, et al.
American Journal of Medical Genetics|August 26, 1998
Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome: clinical and neuropathological observations in a 33-year-old manK Keyvani, W Paulus, H Traupe, et al.
Genomics|May 1, 1989
Human monoamine oxidase A and B genes map to Xp 11.23 and are deleted in a patient with Norrie diseaseN C Lan, C Heinzmann, A Gal, et al.
Human Genetics|March 1, 1989
Gene of X-chromosomal congenital stationary night blindness is closely linked to DXS7 on XpA Gal, A Schinzel, U Orth, et al.
Human Genetics|December 24, 1997
Exclusion of PPEF as the gene causing X-linked juvenile retinoschisisE van de Vosse, B Franco, P van der Bent, et al.
Nature Genetics|October 4, 2000
Mutations in ARHGEF6, encoding a guanine nucleotide exchange factor for Rho GTPases, in patients with X-linked mental retardationK Kutsche, H Yntema, A Brandt, et al.
Pageof 4

Showing results (31-40 of 40) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 40 results.
Nature Genetics|September 1, 1994
Missense rhodopsin mutation in a family with recessive RPG Kumaramanickavel, M Maw, M J Denton, 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.
Nature Genetics|November 4, 2000
Mutations in MERTK, the human orthologue of the RCS rat retinal dystrophy gene, cause retinitis pigmentosaA Gal, Y Li, D A Thompson, et al.
Journal of Medical Genetics|February 1, 1996
Five novel mutations in the L1CAM gene in families with X linked hydrocephalusS M Gu, U Orth, A Veske, et al.
Clinical Genetics|March 22, 2001
Brachytelephalangic dwarfism due to the loss of ARSE and SHOX genes resulting from an X;Y translocationJ Seidel, S Schiller, C Kelbova, et al.
American Journal of Medical Genetics|August 26, 1998
Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome: clinical and neuropathological observations in a 33-year-old manK Keyvani, W Paulus, H Traupe, et al.
Genomics|May 1, 1989
Human monoamine oxidase A and B genes map to Xp 11.23 and are deleted in a patient with Norrie diseaseN C Lan, C Heinzmann, A Gal, et al.
Human Genetics|March 1, 1989
Gene of X-chromosomal congenital stationary night blindness is closely linked to DXS7 on XpA Gal, A Schinzel, U Orth, et al.
Human Genetics|December 24, 1997
Exclusion of PPEF as the gene causing X-linked juvenile retinoschisisE van de Vosse, B Franco, P van der Bent, et al.
Nature Genetics|October 4, 2000
Mutations in ARHGEF6, encoding a guanine nucleotide exchange factor for Rho GTPases, in patients with X-linked mental retardationK Kutsche, H Yntema, A Brandt, et al.
Pageof 4