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American Journal of Medical Genetics. Part A|October 14, 2005
Genetic heterogeneity of deafness phenotypes linked to DFNA4Tao Yang, Markus Pfister, Nikolaus Blin, et al.
Human Genetics|September 12, 2000
Physical mapping and exclusion of GPR34 as the causative gene for congenital stationary night blindness type 1F K Jacobi, M Broghammer, K Pesch, et al.
Human Molecular Genetics|September 6, 2008
Rab8b GTPase, a protein transport regulator, is an interacting partner of otoferlin, defective in a human autosomal recessive deafness formPaulina Heidrych, Ulrike Zimmermann, Andreas Bress, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|October 25, 2002
Phenotypic expression of the complete type of X-linked congenital stationary night blindness in patients with different mutations in the NYX geneFelix K Jacobi, Sten Andréasson, Hana Langrova, et al.
International Journal of Paleopathology|March 15, 2018
Eleonora of Toledo (1522-1562): Evidence for tuberculosis and leishmaniasis co-infection in Renaissance ItalyR Bianucci, V Giuffra, B E Bachmeier, et al.
The Journal of Physiology|December 1, 1996
Concentration and pH dependence of skeletal muscle chloride channel ClC-1G Y Rychkov, M Pusch, D S Astill, et al.
Investigative Ophthalmology & Visual Science|May 1, 2001
Segregation patterns and heteroplasmy prevalence in Leber's hereditary optic neuropathyF K Jacobi, B Leo-Kottler, K Mittelviefhaus, et al.
Investigative Ophthalmology & Visual Science|April 26, 2003
Isolation of the mouse nyctalopin gene nyx and expression studies in mouse and rat retinaKatrin Pesch, Christina Zeitz, Julia E Fries, et al.
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