Showing results (11-20 of 21) with videos related to

Sort By:
Pageof 3
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|May 25, 2001
Clinical electrophysiology of two rod pathways: normative values and clinical applicationH P Scholl, H Langrová, B H Weber, et al.
Journal of the Optical Society of America. A, Optics, Image Science, and Vision|March 9, 2000
L/M cone ratios in human trichromats assessed by psychophysics, electroretinography, and retinal densitometryJ Kremers, H P Scholl, H Knau, et al.
Experimental Cell Research|July 1, 1990
Distribution of chromosome 18 and X centric heterochromatin in the interphase nucleus of cultured human cellsS Popp, H P Scholl, P Loos, et al.
Investigative Ophthalmology & Visual Science|October 3, 2001
Slow and fast rod ERG pathways in patients with X-linked complete stationary night blindness carrying mutations in the NYX geneH P Scholl, H Langrová, C M Pusch, et al.
Pharmacopsychiatry|March 1, 1994
Clinical response to sleep deprivation and auditory-evoked potentials--preliminary resultsP Danos, S Kasper, H P Scholl, et al.
Klinische Monatsblatter Fur Augenheilkunde|October 24, 2007
[Unilateral pigmented paravenous retinochoroidal atrophy]P Charbel Issa, H P Scholl, H-M Helb, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|January 8, 2019
Impact of segmentation density on spectral domain optical coherence tomography assessment in Stargardt diseaseSwetha Bindu Velaga, Muneeswar Gupta Nittala, Dennis Jenkins, et al.
Human Genetics|December 1, 1986
Detection of chromosome aberrations in the human interphase nucleus by visualization of specific target DNAs with radioactive and non-radioactive in situ hybridization techniques: diagnosis of trisomy 18 with probe L1.84T Cremer, J Landegent, A Brückner, et al.
Cytogenetics and Cell Genetics|January 1, 1986
Two subsets of human alphoid repetitive DNA show distinct preferential localization in the pericentric regions of chromosomes 13, 18, and 21P Devilee, T Cremer, P Slagboom, et al.
American Journal of Human Genetics|August 26, 2000
A comprehensive survey of sequence variation in the ABCA4 (ABCR) gene in Stargardt disease and age-related macular degenerationA Rivera, K White, H Stöhr, et al.
Pageof 3