Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Search Results
5 results
Filters applied: . Clear all
Results are displayed in a computed author sort order.
The Results By Year timeline is not available.
Page 1
Screening genes of the retinoid metabolism: novel LRAT mutation in leber congenital amaurosis.
Am J Ophthalmol. 2006 Oct;142(4):702-4. doi: 10.1016/j.ajo.2006.04.057.
Am J Ophthalmol. 2006.
PMID: 17011878
Gene structure, chromosomal localization, and mutation screening of the human gene for the inner ear protein otospiralin.
Lavigne-Rebillard M, Delprat B, Surget MO, Griffoin JM, Weil D, Arbones M, Vincent R, Hamel CP.
Lavigne-Rebillard M, et al. Among authors: surget mo.
Neurogenetics. 2003 Apr;4(3):137-40. doi: 10.1007/s10048-003-0145-0. Epub 2003 Mar 22.
Neurogenetics. 2003.
PMID: 12687421
Item in Clipboard
Relative frequencies of inherited retinal dystrophies and optic neuropathies in Southern France: assessment of 21-year data management.
Bocquet B, Lacroux A, Surget MO, Baudoin C, Marquette V, Manes G, Hebrard M, Sénéchal A, Delettre C, Roux AF, Claustres M, Dhaenens CM, Rozet JM, Perrault I, Bonnefont JP, Kaplan J, Dollfus H, Amati-Bonneau P, Bonneau D, Reynier P, Audo I, Zeitz C, Sahel JA, Paquis-Flucklinger V, Calvas P, Arveiler B, Kohl S, Wissinger B, Blanchet C, Meunier I, Hamel CP.
Bocquet B, et al. Among authors: surget mo.
Ophthalmic Epidemiol. 2013;20(1):13-25. doi: 10.3109/09286586.2012.737890.
Ophthalmic Epidemiol. 2013.
PMID: 23350551
Item in Clipboard
Fourteen novel OPA1 mutations in autosomal dominant optic atrophy including two de novo mutations in sporadic optic atrophy.
Baris O, Delettre C, Amati-Bonneau P, Surget MO, Charlin JF, Catier A, Derieux L, Guyomard JL, Dollfus H, Jonveaux P, Ayuso C, Maumenee I, Lorenz B, Mohammed S, Tourmen Y, Bonneau D, Malthièry Y, Hamel C, Reynier P.
Baris O, et al. Among authors: surget mo.
Hum Mutat. 2003 Jun;21(6):656. doi: 10.1002/humu.9152.
Hum Mutat. 2003.
PMID: 14961560
Item in Clipboard
Phenotypic diversity and mutation spectrum in hypotrichosis with juvenile macular dystrophy.
Indelman M, Hamel CP, Bergman R, Nischal KK, Thompson D, Surget MO, Ramon M, Ganthos H, Miller B, Richard G, Lurie R, Leibu R, Russell-Eggitt I, Sprecher E.
Indelman M, et al. Among authors: surget mo.
J Invest Dermatol. 2003 Nov;121(5):1217-20. doi: 10.1046/j.1523-1747.2003.12550_1.x.
J Invest Dermatol. 2003.
PMID: 14708629
Free article.
Item in Clipboard
Cite
Cite