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Anophthalmia and microphthalmia.
Verma AS, Fitzpatrick DR
Orphanet J Rare Dis 2007, 2:47
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PubMed Central articles that cite the above article:

1.	Identification of novel mutations and sequence variants in the SOX2 and CHX10 genes in patients with anophthalmia/microphthalmia. Zhou J, Kherani F, Bardakjian TM, Katowitz J, Hughes N, Schimmenti LA, Schneider A, Young TL Mol Vis 2008, 14:583-92 [PubMed Central] [PubMed] [Related articles]
2.	Identification of STRA6 and SKI sequence variants in patients with anophthalmia/microphthalmia. White T, Lu T, Metlapally R, Katowitz J, Kherani F, Wang TY, Tran-Viet KN, Young TL Mol Vis 2008, 14:2458-65 [PubMed Central] [PubMed] [Related articles]
3.	Clinical and genetic features of a dominantly-inherited microphthalmia pedigree from China. Yu C, Hu Z, Li J, Liu T, Xia K, Xie L Mol Vis 2009, 15:949-54 [PubMed Central] [PubMed] [Related articles]
4.	An alphaA-crystallin gene mutation, Arg12Cys, causing inherited cataract-microcornea exhibits an altered heat-shock response. Zhang LY, Yam GH, Tam PO, Lai RY, Lam DS, Pang CP, Fan DS Mol Vis 2009, 15:1127-38 [PubMed Central] [PubMed] [Related articles]
5.	Molecular analysis of FOXC1 in subjects presenting with severe developmental eye anomalies. Kaur K, Ragge NK, Ragoussis J Mol Vis 2009, 15:1366-73 [PubMed Central] [PubMed] [Related articles]

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