-
Phenotypic heterogeneity of CYP1B1: mutations in a patient with Peters' anomaly.
Vincent A,
Billingsley G,
Priston M,
Williams-Lyn D,
Sutherland J,
Glaser T,
Oliver E,
Walter MA,
Heathcote G,
Levin A,
Héon E.
PMID: 11403040 [PubMed - indexed for MEDLINE]
PMCID: PMC1734880
-
Cited by 4 PubMed Central articles
-
CYP1B1 mutations in Spanish patients with primary congenital glaucoma: phenotypic and functional variability.
Campos-Mollo E, López-Garrido MP, Blanco-Marchite C, Garcia-Feijoo J, Peralta J, Belmonte-Martínez J, Ayuso C, Escribano J.
Mol Vis. 2009; 15:417-31. Epub 2009 Feb 23.
[Mol Vis. 2009]
-
ReviewGlaucoma genetics.
Challa P.
Int Ophthalmol Clin. 2008 Fall; 48(4):73-94.
[Int Ophthalmol Clin. 2008]
-
Three new PAX6 mutations including one causing an unusual ophthalmic phenotype associated with neurodevelopmental abnormalities.
Dansault A, David G, Schwartz C, Jaliffa C, Vieira V, de la Houssaye G, Bigot K, Catin F, Tattu L, Chopin C, et al.
Mol Vis. 2007 Apr 2; 13:511-23. Epub 2007 Apr 2.
[Mol Vis. 2007]
- » See all...