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9.1.3 Syndromes of Axenfeld, Rieger, Peters, aniridia (2)

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Display all abstracts in classification 9.1.3 Syndromes of Axenfeld, Rieger, Peters, aniridia

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24627 FOXC1 is required for normal cerebellar development and is a major contributor to chromosome 6p25.3 Dandy-Walker malformation
Aldinger KA; Lehmann OJ; Hudgins L; Chizhikov VV; Bassuk AG; Ades LC; Krantz ID; Dobyns WB; Millen KJ
Nature Genetics 2009; 41: 1037-1042
24639 Sequence analysis of MYOC and CYP1B1 in a Chinese pedigree of juvenile glaucoma with goniodysgenesis
Chen X; Yan N; Yun H; Sun J; Yu M; Zhou J; Cao G; Yin H; Li M; Liu X
Molecular Vision 2009; 15: 1530-1536

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