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American Journal of Ophthalmology|April 9, 2001
Autosomal dominant inheritance of a negative electroretinogram phenotype in three generationsK M Fitzgerald, T Hashimoto, T E Hug, et al.
Journal of Evolutionary Biology|June 4, 2014
Evolution of alternative male morphotypes in oxyurid nematodes: a case of convergence?F Jorge, A Perera, V Roca, et al.
Journal of Applied Physiology: Respiratory, Environmental and Exercise Physiology|April 1, 1983
Liquid ventilation in dogs: an apparatus for normobaric and hyperbaric studiesD J Harris, R R Coggin, J Roby, et al.
American Journal of Diseases of Children (1960)|August 1, 1981
Mucolipidosis I (acid neuraminidase deficiency). Three cases and delineation of the variability of the phenotypeT E Kelly, L Bartoshesky, D J Harris, et al.
American Journal of Human Genetics|June 1, 1995
Evidence for a distinct region causing a cat-like cry in patients with 5p deletionsM Gersh, S A Goodart, L M Pasztor, et al.
Ophthalmology|August 1, 1986
Lenticular opacities in carriers of Lowe's syndromeG W Cibis, J M Waeltermann, C T Whitcraft, et al.
The American Journal of Cardiology|April 15, 1996
Comparison and reproducibility of visual echocardiographic and quantitative radionuclide left ventricular ejection fractionsN van Royen, C C Jaffe, H M Krumholz, et al.
The New England Journal of Medicine|March 11, 1982
Fetal echocardiography for evaluation of in utero congestive heart failureC S Kleinman, R L Donnerstein, G R DeVore, et al.
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