Bilateral epiretinal membranes in Gorlin syndrome associated with a novel PTCH mutation.
about
Review of Ocular Manifestations of Nevoid Basal Cell Carcinoma Syndrome: What an Ophthalmologist Needs to KnowDensity of common complex ocular traits in the aging eye: analysis of secondary traits in genome-wide association studiesNovel patched 1 mutations in patients with nevoid basal cell carcinoma syndrome--case report.Mutations in BMP4 cause eye, brain, and digit developmental anomalies: overlap between the BMP4 and hedgehog signaling pathways.Combined Hamartoma of the Retina and Retinal Pigment Epithelium in a Patient with Gorlin Syndrome: Spontaneous Partial Resolution of Traction Caused by Epiretinal Membrane.
P2860
Bilateral epiretinal membranes in Gorlin syndrome associated with a novel PTCH mutation.
description
2006 nî lūn-bûn
@nan
2006年の論文
@ja
2006年学术文章
@wuu
2006年学术文章
@zh-cn
2006年学术文章
@zh-hans
2006年学术文章
@zh-my
2006年学术文章
@zh-sg
2006年學術文章
@yue
2006年學術文章
@zh
2006年學術文章
@zh-hant
name
Bilateral epiretinal membranes in Gorlin syndrome associated with a novel PTCH mutation.
@en
Bilateral epiretinal membranes in Gorlin syndrome associated with a novel PTCH mutation.
@nl
type
label
Bilateral epiretinal membranes in Gorlin syndrome associated with a novel PTCH mutation.
@en
Bilateral epiretinal membranes in Gorlin syndrome associated with a novel PTCH mutation.
@nl
prefLabel
Bilateral epiretinal membranes in Gorlin syndrome associated with a novel PTCH mutation.
@en
Bilateral epiretinal membranes in Gorlin syndrome associated with a novel PTCH mutation.
@nl
P2093
P1476
Bilateral epiretinal membranes in Gorlin syndrome associated with a novel PTCH mutation
@en
P2093
Andrew Scott
Eamonn R Maher
Joan Forsyth
Michel Michaelides
Nicholas G Strouthidis
Patricio G Schlottmann
P304
P356
10.1016/J.AJO.2006.09.022
P407
P50
P577
2006-10-23T00:00:00Z