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L F Raymond

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Annals of Ophthalmology|April 1, 1975
Physiology of color vision and the pathological changes in reversible color blindness, a deficiency disease of the retinaL F Raymond
Eye, Ear, Nose & Throat Monthly|April 1, 1972
Color-blindness-deficiency disease, auto-immune, or sex-linked inherited deficiency diseaseL F Raymond
Annals of Allergy|April 1, 1971
Color blindnessL F Raymond
Clinical Genetics|August 19, 2014
Phenotypic spectrum associated with PTCHD1 deletions and truncating mutations includes intellectual disability and autism spectrum disorderA Chaudhry, A Noor, B Degagne, et al.
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Showing results (1-10 of 4) with videos related to

Sort By:
Pageof 1
Annals of Ophthalmology|April 1, 1975
Physiology of color vision and the pathological changes in reversible color blindness, a deficiency disease of the retinaL F Raymond
Eye, Ear, Nose & Throat Monthly|April 1, 1972
Color-blindness-deficiency disease, auto-immune, or sex-linked inherited deficiency diseaseL F Raymond
Annals of Allergy|April 1, 1971
Color blindnessL F Raymond
Clinical Genetics|August 19, 2014
Phenotypic spectrum associated with PTCHD1 deletions and truncating mutations includes intellectual disability and autism spectrum disorderA Chaudhry, A Noor, B Degagne, et al.
Pageof 1