Associated Papers
A novel FOXF1 mutation associated with alveolar capillary dysplasia and coexisting colobomas and hemihyperplasia.
Geddes GC et al.
Journal of Perinatology : Official Journal of the California Perinatal Association, 2015
Identification of STRA6 and SKI sequence variants in patients with anophthalmia/microphthalmia.
White T et al.
Molecular Vision, 2008
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