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K Steindl

Showing results (1-10 of 12) with videos related to

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American Journal of Medical Genetics|May 5, 2001
New syndrome of mental retardation, Robin sequence, and brachydactylyF Gurrieri, K Steindl, S Giglio, et al.
American Journal of Medical Genetics|October 22, 1998
Nonsyndromal overgrowth in males with mild psychomotor delayG Neri, K Steindl, A Mazzei, et al.
Mutation Research|July 1, 1993
Karyotype modifications in human malignant melanoma cell cultures after treatment with azelaic acidP Grammatico, S Scarpa, M Picardo, et al.
Cancer Genetics and Cytogenetics|June 1, 1992
Lentigo maligna. Cytogenetic, ultrastructural, and phenotypic characterization of a primary cell cultureP Grammatico, A Modesti, K Steindl, et al.
European Journal of Human Genetics : EJHG|November 28, 2000
Two novel mutations confirm FGD1 is responsible for the Aarskog syndromeC E Schwartz, G Gillessen-Kaesbach, M May, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|January 1, 1995
Correlation between Goldmann perimetry and maximal electroretinogram response in retinitis pigmentosaA Iannaccone, E Rispoli, E M Vingolo, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|December 1, 1994
Clinical heterogeneity of dominant optic atrophy: the contribution of visual function investigations to diagnosisG Del Porto, E M Vingolo, K Steindl, et al.
Eye (London, England)|January 27, 2009
Complement factor H gene polymorphisms and Chlamydia pneumoniae infection in age-related macular degenerationP Haas, K Steindl, K E Schmid-Kubista, et al.
Journal of Medical Genetics|September 1, 1994
Autosomal dominant simple microphthalmosE M Vingolo, K Steindl, R Forte, et al.
Clinical Genetics|November 4, 2010
A novel C2orf37 mutation causes the first Italian cases of Woodhouse Sakati syndromeK Steindl, A M Alazami, K P Bhatia, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
American Journal of Medical Genetics|May 5, 2001
New syndrome of mental retardation, Robin sequence, and brachydactylyF Gurrieri, K Steindl, S Giglio, et al.
American Journal of Medical Genetics|October 22, 1998
Nonsyndromal overgrowth in males with mild psychomotor delayG Neri, K Steindl, A Mazzei, et al.
Mutation Research|July 1, 1993
Karyotype modifications in human malignant melanoma cell cultures after treatment with azelaic acidP Grammatico, S Scarpa, M Picardo, et al.
Cancer Genetics and Cytogenetics|June 1, 1992
Lentigo maligna. Cytogenetic, ultrastructural, and phenotypic characterization of a primary cell cultureP Grammatico, A Modesti, K Steindl, et al.
European Journal of Human Genetics : EJHG|November 28, 2000
Two novel mutations confirm FGD1 is responsible for the Aarskog syndromeC E Schwartz, G Gillessen-Kaesbach, M May, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|January 1, 1995
Correlation between Goldmann perimetry and maximal electroretinogram response in retinitis pigmentosaA Iannaccone, E Rispoli, E M Vingolo, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|December 1, 1994
Clinical heterogeneity of dominant optic atrophy: the contribution of visual function investigations to diagnosisG Del Porto, E M Vingolo, K Steindl, et al.
Eye (London, England)|January 27, 2009
Complement factor H gene polymorphisms and Chlamydia pneumoniae infection in age-related macular degenerationP Haas, K Steindl, K E Schmid-Kubista, et al.
Journal of Medical Genetics|September 1, 1994
Autosomal dominant simple microphthalmosE M Vingolo, K Steindl, R Forte, et al.
Clinical Genetics|November 4, 2010
A novel C2orf37 mutation causes the first Italian cases of Woodhouse Sakati syndromeK Steindl, A M Alazami, K P Bhatia, et al.
Pageof 2