Results 111 to 120 of about 12,123 (207)
Intragenic loss-of-function variants in transcription factors <i>MAZ</i>, <i>FOXP1</i> and <i>SIN3B</i> in colobomatous microphthalmia. [PDF]
Seese SE +4 more
europepmc +1 more source
Isolated Lenticular Coloboma in an Atypical Location With Early Cataract Formation: A Case Report. [PDF]
Noori SH, Nomikarios M, Anikina E.
europepmc +1 more source
Limb-Body wall complex with anophthalmos and choroidal coloboma
Øjensygdomme, limb-body wall complex, ocular malformations, choroidal coloboma ...
Löfgren, O. +3 more
core
Atypical superotemporal iris and retinal coloboma. [PDF]
Patterson KN, Reynolds MM, Lueder GT.
europepmc +1 more source
Variants in the CxxC domain of the epigenetic regulator KDM2B support its role in developmental eye anomalies. [PDF]
Ceroni F +12 more
europepmc +1 more source
ABCA4-associated maculopathy suspected to be ocular toxoplasmosis. [PDF]
Elsayed MEAA, Barone V, MacLaren RE.
europepmc +1 more source
Expanded Phenotype of PAX2-Related Papillorenal Syndrome: A Case Featuring FSGS, Atypical Retinopathy, Cerebellar Hypoplasia, and ADHD. [PDF]
Sultana N, Mamun AA, Begum A.
europepmc +1 more source

