Matches in Nanopublications for { ?s ?p "[Patients with either RGS9/R9AP mutations (bradyopsia) or oligocone trichromacy have very similar clinical phenotypes, characterized by stationary cone dysfunction, mild photophobia, normal color vision, lack of nystagmus, and normal fundi.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP224839.RASVC47BD1iAnsFvNpWQRNL_VgHBKBD5bIphgNKDIgtJ4130_assertion description "[Patients with either RGS9/R9AP mutations (bradyopsia) or oligocone trichromacy have very similar clinical phenotypes, characterized by stationary cone dysfunction, mild photophobia, normal color vision, lack of nystagmus, and normal fundi.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP224839.RASVC47BD1iAnsFvNpWQRNL_VgHBKBD5bIphgNKDIgtJ4130_provenance.
- NP433973.RACPIEq4xRVnr6UPfwhOXHvF2Ph2-gx5N3lBWMY21PnQU130_assertion description "[Patients with either RGS9/R9AP mutations (bradyopsia) or oligocone trichromacy have very similar clinical phenotypes, characterized by stationary cone dysfunction, mild photophobia, normal color vision, lack of nystagmus, and normal fundi.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP433973.RACPIEq4xRVnr6UPfwhOXHvF2Ph2-gx5N3lBWMY21PnQU130_provenance.
- NP742538.RAwrSL9bM-ZTvK34zAGbAZ7ASSkku2WdXTpf2sHJheVkI130_assertion description "[Patients with either RGS9/R9AP mutations (bradyopsia) or oligocone trichromacy have very similar clinical phenotypes, characterized by stationary cone dysfunction, mild photophobia, normal color vision, lack of nystagmus, and normal fundi.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP742538.RAwrSL9bM-ZTvK34zAGbAZ7ASSkku2WdXTpf2sHJheVkI130_provenance.
- NP764669.RA4XCGE1gBkQbnudWssLlKJrBGd1hI72NJhRzsYe94dUI130_assertion description "[Patients with either RGS9/R9AP mutations (bradyopsia) or oligocone trichromacy have very similar clinical phenotypes, characterized by stationary cone dysfunction, mild photophobia, normal color vision, lack of nystagmus, and normal fundi.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP764669.RA4XCGE1gBkQbnudWssLlKJrBGd1hI72NJhRzsYe94dUI130_provenance.
- NP768615.RAVs4r1TYErULma4ksFwkIloVTjJiVyEH_wg7cyHzfQpU130_assertion description "[Patients with either RGS9/R9AP mutations (bradyopsia) or oligocone trichromacy have very similar clinical phenotypes, characterized by stationary cone dysfunction, mild photophobia, normal color vision, lack of nystagmus, and normal fundi.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP768615.RAVs4r1TYErULma4ksFwkIloVTjJiVyEH_wg7cyHzfQpU130_provenance.
- NP990281.RArmy_3ait9ossZUCnm7QEQyZbW1QJCFb5c6NqaFv5bV8130_assertion description "[Patients with either RGS9/R9AP mutations (bradyopsia) or oligocone trichromacy have very similar clinical phenotypes, characterized by stationary cone dysfunction, mild photophobia, normal color vision, lack of nystagmus, and normal fundi.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP990281.RArmy_3ait9ossZUCnm7QEQyZbW1QJCFb5c6NqaFv5bV8130_provenance.
- NP768616.RAnGzcy8-C9mwPoJW2HbUPec_mTMgGg8_ZB-dXCdUXLL0130_assertion description "[Patients with either RGS9/R9AP mutations (bradyopsia) or oligocone trichromacy have very similar clinical phenotypes, characterized by stationary cone dysfunction, mild photophobia, normal color vision, lack of nystagmus, and normal fundi.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP768616.RAnGzcy8-C9mwPoJW2HbUPec_mTMgGg8_ZB-dXCdUXLL0130_provenance.
- NP990276.RA7aWcjDagsOO84o_kW7Slk3TEQPTeJ-Kno_dVuxJJBg4130_assertion description "[Patients with either RGS9/R9AP mutations (bradyopsia) or oligocone trichromacy have very similar clinical phenotypes, characterized by stationary cone dysfunction, mild photophobia, normal color vision, lack of nystagmus, and normal fundi.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP990276.RA7aWcjDagsOO84o_kW7Slk3TEQPTeJ-Kno_dVuxJJBg4130_provenance.