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Current Opinion in Ophthalmology
|
July 30, 2013
Lyonization in ophthalmology
Wadakarn Wuthisiri, Michelle D Lingao, Jenina E Capasso, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus
|
April 5, 2014
Anterior lentiplane associated with posterior lenticonus and microcornea
Michelle D Lingao, Grace T Liu, Kammi Gunton, et al.
Ophthalmic Genetics
|
August 20, 2020
Novel compound heterozygous pathogenic <i>BBS5</i> variants in Filipino siblings with Bardet-Biedl syndrome (BBS)
Aramis B Torrefranca, Alvina Pauline D Santiago, Michelle D Lingao, et al.
Ophthalmic Genetics
|
November 28, 2022
Isolated aniridia caused by a novel <i>PAX6</i> heterozygous deletion mediated by multi-exon complex rearrangement
Aramis B Torrefranca, Suzanne Marie Carmona, Alvina Pauline D Santiago, et al.
Oman Journal of Ophthalmology
|
March 26, 2016
Organophosphate retinopathy
Hang Pham, Michelle D Lingao, Anuradha Ganesh, et al.
Ophthalmology
|
August 27, 2013
Ocular manifestations of 22q11.2 microduplication
Jose A Cordovez, Jenina Capasso, Michelle D Lingao, et al.
Ophthalmic Genetics
|
February 20, 2016
Macular cystoid spaces in patients with retinal dystrophy
Michelle D Lingao, Anuradha Ganesh, Arcot S Karthikeyan, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 7) with videos related to
Sort By:
Page
of 1
Current Opinion in Ophthalmology
|
July 30, 2013
Lyonization in ophthalmology
Wadakarn Wuthisiri, Michelle D Lingao, Jenina E Capasso, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus
|
April 5, 2014
Anterior lentiplane associated with posterior lenticonus and microcornea
Michelle D Lingao, Grace T Liu, Kammi Gunton, et al.
Ophthalmic Genetics
|
August 20, 2020
Novel compound heterozygous pathogenic <i>BBS5</i> variants in Filipino siblings with Bardet-Biedl syndrome (BBS)
Aramis B Torrefranca, Alvina Pauline D Santiago, Michelle D Lingao, et al.
Ophthalmic Genetics
|
November 28, 2022
Isolated aniridia caused by a novel <i>PAX6</i> heterozygous deletion mediated by multi-exon complex rearrangement
Aramis B Torrefranca, Suzanne Marie Carmona, Alvina Pauline D Santiago, et al.
Oman Journal of Ophthalmology
|
March 26, 2016
Organophosphate retinopathy
Hang Pham, Michelle D Lingao, Anuradha Ganesh, et al.
Ophthalmology
|
August 27, 2013
Ocular manifestations of 22q11.2 microduplication
Jose A Cordovez, Jenina Capasso, Michelle D Lingao, et al.
Ophthalmic Genetics
|
February 20, 2016
Macular cystoid spaces in patients with retinal dystrophy
Michelle D Lingao, Anuradha Ganesh, Arcot S Karthikeyan, et al.
Page
of 1