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A family with Axenfeld–Rieger syndrome and Peters Anomaly caused by a point mutation (Phe112Ser) in the FOXC1 gene
Robert A Honkanen, Darryl Y Nishimura, Ruth E Swiderski, Steven R Bennett, Sungpyo Hong, Young H Kwon, Edwin M Stone, Val C Sheffield, Wallace L.M AlwardVolume:
135
Year:
2003
Language:
english
DOI:
10.1016/s0002-9394(02)02061-5
File:
PDF, 410 KB
english, 2003