Lin P, Hung J, Huang Y
CMAJ. 2024; 196(17):E610-E611.
PMID: 38719218
PMC: 11073823.
DOI: 10.1503/cmaj.231616-f.
Lin P, Hung J, Huang Y
CMAJ. 2024; 196(9):E296.
PMID: 38467409
PMC: 10927287.
DOI: 10.1503/cmaj.231616.
Strauch C, Naber M
Invest Ophthalmol Vis Sci. 2022; 63(2):20.
PMID: 35142787
PMC: 8842542.
DOI: 10.1167/iovs.63.2.20.
Krohn J, Sundal K, Froystein T
BMC Ophthalmol. 2022; 22(1):6.
PMID: 34980044
PMC: 8725464.
DOI: 10.1186/s12886-021-02236-3.
Colman K, Andrews R, Atkins H, Boulineau T, Bradley A, Braendli-Baiocco A
J Toxicol Pathol. 2021; 34(3 Suppl):1S-182S.
PMID: 34712008
PMC: 8544165.
DOI: 10.1293/tox.34.1S.
A case of unilateral sectoral iris heterochromia in an infant with Beckwith-Wiedemann syndrome.
Alnefaie M, Jefri M, Almahmoudi F
Am J Ophthalmol Case Rep. 2021; 23:101150.
PMID: 34189344
PMC: 8220324.
DOI: 10.1016/j.ajoc.2021.101150.
Heterochromia Iridum with Sudden Vision Loss in an Elderly Man - A Trick to Treat.
Panda B, Kanungo S, Nanda A
J Emerg Trauma Shock. 2021; 14(1):56-57.
PMID: 33911441
PMC: 8054803.
DOI: 10.4103/JETS.JETS_108_20.
A novel mutation of the StAR gene with congenital adrenal hyperplasia and its association with heterochromia iridis: a case report.
Splittstosser V, Schreiner F, Gohlke B, Welzel M, Holterhus P, Woelfle J
BMC Endocr Disord. 2019; 19(1):116.
PMID: 31666050
PMC: 6821031.
DOI: 10.1186/s12902-019-0448-2.
[Clinico-echographic diagnostics of iris tumors].
Koch K, Mor J, Avgitidou G, Kakkassery V, Rokohl A, Heindl L
Ophthalmologe. 2019; 116(4):313-323.
PMID: 30778665
DOI: 10.1007/s00347-019-0861-y.
The genetic architecture of aniridia and Gillespie syndrome.
Hall H, Williamson K, Fitzpatrick D
Hum Genet. 2018; 138(8-9):881-898.
PMID: 30242502
PMC: 6710220.
DOI: 10.1007/s00439-018-1934-8.
Iris Hypoplasia as the Presenting Sign of Retinoblastoma in a Child With a 13q Deletion.
Shah S, Koban Y, Le B, Bechtold M, Zolfaghari E, Kim J
J Pediatr Ophthalmol Strabismus. 2018; 55:e10-e13.
PMID: 29684226
PMC: 7444716.
DOI: 10.3928/01913913-20180215-02.
A genome-wide association study reveals a locus for bilateral iridal hypopigmentation in Holstein Friesian cattle.
Hollmann A, Bleyer M, Tipold A, Nessler J, Wemheuer W, Schutz E
BMC Genet. 2017; 18(1):30.
PMID: 28356055
PMC: 5372310.
DOI: 10.1186/s12863-017-0496-4.
Post-thyroidectomy iatrogenic Horner's syndrome with heterochromia.
Ulusoy M, Kivanc S, Atakan M, Mayali H
J Curr Ophthalmol. 2016; 28(1):46-7.
PMID: 27239603
PMC: 4881223.
DOI: 10.1016/j.joco.2016.02.004.
Analysis of iris surface features in populations of diverse ancestry.
Edwards M, Cha D, Krithika S, Johnson M, Parra E
R Soc Open Sci. 2016; 3(1):150424.
PMID: 26909168
PMC: 4736923.
DOI: 10.1098/rsos.150424.
Genetics of eye colours in different rural populations on the Silk Road.
Ulivi S, Mezzavilla M, Gasparini P
Eur J Hum Genet. 2013; 21(11):1320-3.
PMID: 23486544
PMC: 3798846.
DOI: 10.1038/ejhg.2013.41.