Molecular analysis of FOXC1 in subjects presenting with severe developmental eye anomalies
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PITX2 and FOXC1 spectrum of mutations in ocular syndromesAbsence of NR2E1 mutations in patients with aniridia.Rare FOXC1 variants in congenital glaucoma: identification of translation regulatory sequences.Cell Behaviors during Closure of the Choroid Fissure in the Developing Eye.Research progress on the forkhead box C1.
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Molecular analysis of FOXC1 in subjects presenting with severe developmental eye anomalies
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article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on 13 July 2009
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
Molecular analysis of FOXC1 in ...... re developmental eye anomalies
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Molecular analysis of FOXC1 in ...... e developmental eye anomalies.
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Molecular analysis of FOXC1 in ...... re developmental eye anomalies
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Molecular analysis of FOXC1 in ...... e developmental eye anomalies.
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Molecular analysis of FOXC1 in ...... re developmental eye anomalies
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Molecular analysis of FOXC1 in ...... e developmental eye anomalies.
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Molecular analysis of FOXC1 in ...... re developmental eye anomalies
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Jiannis Ragoussis
Kulvinder Kaur
Nicola K Ragge
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P304
P577
2009-07-13T00:00:00Z