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Gregg T Lueder

Showing results (51-60 of 55) with videos related to

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The British Journal of Ophthalmology|May 1, 2015
Retinal degeneration in autoimmune polyglandular syndrome type 1: a case seriesSerge Bourgault, Catherine Baril, Ajoy Vincent, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|May 8, 2010
Periocular granuloma annulare in four childrenInge De Becker, C Gail Summers, Valda Kaye, et al.
American Journal of Medical Genetics. Part A|June 4, 2014
Brain MRI abnormalities and spectrum of neurological and clinical findings in three patients with proximal 16p11.2 microduplicationIsabel Filges, Steven Sparagana, Michael Sargent, et al.
American Journal of Medical Genetics. Part A|April 27, 2004
Severe subacute GM2 gangliosidosis caused by an apparently silent HEXA mutation (V324V) that results in aberrant splicing and reduced HEXA mRNABrandy A Wicklow, Jennifer L Ivanovich, Margot M Plews, et al.
Ophthalmology. Glaucoma|November 28, 2025
Glaucoma Management in Sturge-Weber Syndrome Using the Delphi ProcessKinza Abbas, Bailey Harrison, Ta Chen Peter Chang, et al.
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Showing results (51-60 of 55) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 55 results.
The British Journal of Ophthalmology|May 1, 2015
Retinal degeneration in autoimmune polyglandular syndrome type 1: a case seriesSerge Bourgault, Catherine Baril, Ajoy Vincent, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|May 8, 2010
Periocular granuloma annulare in four childrenInge De Becker, C Gail Summers, Valda Kaye, et al.
American Journal of Medical Genetics. Part A|June 4, 2014
Brain MRI abnormalities and spectrum of neurological and clinical findings in three patients with proximal 16p11.2 microduplicationIsabel Filges, Steven Sparagana, Michael Sargent, et al.
American Journal of Medical Genetics. Part A|April 27, 2004
Severe subacute GM2 gangliosidosis caused by an apparently silent HEXA mutation (V324V) that results in aberrant splicing and reduced HEXA mRNABrandy A Wicklow, Jennifer L Ivanovich, Margot M Plews, et al.
Ophthalmology. Glaucoma|November 28, 2025
Glaucoma Management in Sturge-Weber Syndrome Using the Delphi ProcessKinza Abbas, Bailey Harrison, Ta Chen Peter Chang, et al.
Pageof 6