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We performed mutation analysis in one reported patient 2 and two undescribed patients with OFCD syndrome, as well as in eight patients affected with Lenz microphthalmia syndrome, to confirm that ...
Bosma arhinia microphthalmia syndrome or BAMS is an extremely rare condition associated with facial abnormalities, mainly of the nose and the eye. Mutations in the SMCHD1 gene are the most common ...
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