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U Felbor

Showing results (11-20 of 24) with videos related to

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Nature Genetics|December 1, 1994
Mutations in the tissue inhibitor of metalloproteinases-3 (TIMP3) in patients with Sorsby's fundus dystrophyB H Weber, G Vogt, R C Pruett, et al.
Cytogenetic and Genome Research|June 26, 2004
Mosaicism for an ectopic NOR at 8pter and a complex rearrangement of chromosome 8 in a patient with severe psychomotor retardationU Felbor, N Knötgen, G Schams, et al.
Der Internist|May 17, 2013
[Mild bleeding diathesis in a 62-year-old woman with hereditary thrombocytopenia]R Ventz, M Hundemer, M Witzens-Harig, et al.
American Journal of Human Genetics|January 1, 1997
Autosomal recessive Sorsby fundus dystrophy revisited: molecular evidence for dominant inheritanceU Felbor, E A Suvanto, H R Forsius, et al.
Journal of Medical Genetics|March 1, 1996
A second independent Tyr168Cys mutation in the tissue inhibitor of metalloproteinases-3 (TIMP3) in Sorsby's fundus dystrophyU Felbor, H Stöhr, T Amann, et al.
The EMBO Journal|March 16, 2000
Secreted cathepsin L generates endostatin from collagen XVIIIU Felbor, L Dreier, R A Bryant, et al.
Neurogenetics|January 11, 2007
Large germline deletions and duplication in isolated cerebral cavernous malformation patientsU Felbor, S Gaetzner, D J Verlaan, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|December 24, 1997
Sorsby fundus dystrophy: reevaluation of variable expressivity in patients carrying a TIMP3 founder mutationU Felbor, C Benkwitz, M L Klein, et al.
Cytogenetics and Cell Genetics|August 6, 1998
Genomic organization and chromosomal localization of the interphotoreceptor matrix proteoglycan-1 (IMPG1) gene: a candidate for 6q-linked retinopathiesU Felbor, A Gehrig, C G Sauer, et al.
Journal of Medical Genetics|August 27, 1998
Assessment of the interphotoreceptor matrix proteoglycan-1 (IMPG1) gene localised to 6q13-q15 in autosomal dominant Stargardt-like disease (ADSTGD), progressive bifocal chorioretinal atrophy (PBCRA), and North Carolina macular dystrophy (MCDR1)A Gehrig, U Felbor, R E Kelsell, et al.
Pageof 3

Showing results (11-20 of 24) with videos related to

Sort By:
Pageof 3
Nature Genetics|December 1, 1994
Mutations in the tissue inhibitor of metalloproteinases-3 (TIMP3) in patients with Sorsby's fundus dystrophyB H Weber, G Vogt, R C Pruett, et al.
Cytogenetic and Genome Research|June 26, 2004
Mosaicism for an ectopic NOR at 8pter and a complex rearrangement of chromosome 8 in a patient with severe psychomotor retardationU Felbor, N Knötgen, G Schams, et al.
Der Internist|May 17, 2013
[Mild bleeding diathesis in a 62-year-old woman with hereditary thrombocytopenia]R Ventz, M Hundemer, M Witzens-Harig, et al.
American Journal of Human Genetics|January 1, 1997
Autosomal recessive Sorsby fundus dystrophy revisited: molecular evidence for dominant inheritanceU Felbor, E A Suvanto, H R Forsius, et al.
Journal of Medical Genetics|March 1, 1996
A second independent Tyr168Cys mutation in the tissue inhibitor of metalloproteinases-3 (TIMP3) in Sorsby's fundus dystrophyU Felbor, H Stöhr, T Amann, et al.
The EMBO Journal|March 16, 2000
Secreted cathepsin L generates endostatin from collagen XVIIIU Felbor, L Dreier, R A Bryant, et al.
Neurogenetics|January 11, 2007
Large germline deletions and duplication in isolated cerebral cavernous malformation patientsU Felbor, S Gaetzner, D J Verlaan, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|December 24, 1997
Sorsby fundus dystrophy: reevaluation of variable expressivity in patients carrying a TIMP3 founder mutationU Felbor, C Benkwitz, M L Klein, et al.
Cytogenetics and Cell Genetics|August 6, 1998
Genomic organization and chromosomal localization of the interphotoreceptor matrix proteoglycan-1 (IMPG1) gene: a candidate for 6q-linked retinopathiesU Felbor, A Gehrig, C G Sauer, et al.
Journal of Medical Genetics|August 27, 1998
Assessment of the interphotoreceptor matrix proteoglycan-1 (IMPG1) gene localised to 6q13-q15 in autosomal dominant Stargardt-like disease (ADSTGD), progressive bifocal chorioretinal atrophy (PBCRA), and North Carolina macular dystrophy (MCDR1)A Gehrig, U Felbor, R E Kelsell, et al.
Pageof 3