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Journal of Pediatric Ophthalmology and Strabismus|January 1, 1982
Autosomal dominant ophthalmologic disorders and linkageH M Hittner, R E FerrellAmerican Journal of Medical Genetics|January 1, 1981
Autosomal dominant cone-rod dystrophy: a linkage study with 17 biochemical and serological markersR E Ferrell, H M Hittner, A ChakravartiAmerican Journal of Human Genetics|January 1, 1983
Linkage of atypical vitelliform macular dystrophy (VMD-1) to the soluble glutamate pyruvate transaminase (GPT1) locusR E Ferrell, H M Hittner, J H AntoszykThe British Journal of Ophthalmology|March 1, 1984
Atypical vitelliform macular dystrophy in a 5-generation familyH M Hittner, R E Ferrell, R P Borda, et al.Proceedings of the National Academy of Sciences of the United States of America|March 1, 1980
Autosomal dominant aniridia: probable linkage to acid phosphatase-1 locus on chromosome 2R E Ferrell, A Chakravarti, H M Hittner, et al.American Journal of Human Genetics|March 1, 1982
Anterior segment mesenchymal dysgenesis: probable linkage to the MNS blood group on chromosome 4R E Ferrell, H M Hittner, F L Kretzer, et al.American Journal of Ophthalmology|April 1, 1980
Variable expressivity in autosomal dominant aniridia by clinical, electrophysiologic, and angiographic criteriaH M Hittner, V M Riccardi, R E Ferrell, et al.American Journal of Ophthalmology|January 1, 1982
Variable expressivity of autosomal dominant anterior segment mesenchymal dysgenesis in six generationsH M Hittner, F L Kretzer, J H Antoszyk, et al.The Journal of Pediatrics|April 1, 1982
Wilms tumor with aniridia/iris dysplasia and apparently normal chromosomesV M Riccardi, H M Hittner, L C Strong, et al.Pageof 36