Congenital diaphragmatic hernia.
Zani A, Chung WK, Deprest J, Harting MT, Jancelewicz T, Kunisaki SM, Patel N, Antounians L, Puligandla PS, Keijzer R.
Nat Rev Dis Primers. 2022 Jun 1;8(1):37. doi: 10.1038/s41572-022-00362-w.
Peter's anomaly-A homeotic gene disorder.
Kylat RI.
Acta Paediatr. 2022 May;111(5):948-951. doi: 10.1111/apa.16260. Epub 2022 Jan 31.
In reply.
Van Mieghem T, Klaritsch P, Raio L, Ranzini AC, Baud D, Barrett J, De Heus R, Ryan G.
Obstet Gynecol. 2015 Jan;125(1):228-229. doi: 10.1097/AOG.0000000000000613.
Peter's anomaly.
Smith GM, Velzeboer CM.
Ophthalmologica. 1975;171(4-5):318-20. doi: 10.1159/000307538.
PAX6 mutations reviewed.
Prosser J, van Heyningen V.
Hum Mutat. 1998;11(2):93-108. doi: 10.1002/(SICI)1098-1004(1998)11:2<93::AID-HUMU1>3.0.CO;2-M.
[Late diagnosis of Peter's anomaly type 1].
Dambricourt L, Gonzalvez M, Levy N, Denis D, David T.
J Fr Ophtalmol. 2022 Mar;45(3):360-362. doi: 10.1016/j.jfo.2021.09.018. Epub 2022 Jan 29.
A case with cardiac, skeletal, speech, and motor traits narrows the subtelomeric 19p13.3 microdeletion region to 46 kb.
Peter B.
Am J Med Genet A. 2023 Jan;191(1):120-129. doi: 10.1002/ajmg.a.62998. Epub 2022 Oct 22.
Ocular Phenotype of Peters-Plus Syndrome.
Shah PR, Chauhan B, Chu CT, Kofler J, Nischal KK.
Cornea. 2022 Feb 1;41(2):219-223. doi: 10.1097/ICO.0000000000002889.
Atypical and Asymmetric Peter's Anomaly.
Sihota Md R, Mahalingam K, Rakheja Md V.
Ophthalmol Glaucoma. 2021 Sep-Oct;4(5):503. doi: 10.1016/j.ogla.2021.04.005.
Interstitial deletion 2q14q21.
Frydman M, Steinberger J, Shabtai F, Katznelson MB, Varsano I.
Am J Med Genet. 1989 Dec;34(4):476-9. doi: 10.1002/ajmg.1320340405.
