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Axenfeld–Rieger syndrome and spectrum of PITX2 and FOXC1 mutations | European Journal of Human Genetics
The Molecular Basis of Rieger Syndrome - Journal of Biological Chemistry
Dein Möbelhaus in Esslingen bei Stuttgart | Möbel RIEGER
Dein Möbelhaus in Esslingen bei Stuttgart | Möbel RIEGER
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Towards chemistry at absolute zero | Nature Reviews Chemistry
A family with Axenfeld–Rieger syndrome and Peters Anomaly caused by a point mutation (Phe112Ser) in the FOXC1 gene - American Journal of Ophthalmology
CH3)Al(CH2)]12: Methylaluminomethylene (MAM‐12) - Spiridopoulos - 2022 - Chemistry – A European Journal - Wiley Online Library
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Axenfeld–Rieger syndrome and spectrum of PITX2 and FOXC1 mutations | European Journal of Human Genetics
Clinical features of Axenfeld – Rieger malformations. ( A ) Slate-gray,... | Download Scientific Diagram
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