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Human microphthalmia associated with mutations in the retinal homeobox gene CHX10.
Nat Genet. 2000 Aug;25(4):397-401. doi: 10.1038/78071.
Nat Genet. 2000.
PMID: 10932181
Mutations in the CHX10 gene in non-syndromic microphthalmia/anophthalmia patients from Qatar.
Faiyaz-Ul-Haque M, Zaidi SH, Al-Mureikhi MS, Peltekova I, Tsui LC, Teebi AS.
Faiyaz-Ul-Haque M, et al.
Clin Genet. 2007 Aug;72(2):164-6. doi: 10.1111/j.1399-0004.2007.00846.x.
Clin Genet. 2007.
PMID: 17661825
No abstract available.
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