DOI:
10.1055/s-00029027
Journal of Pediatric Genetics
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References
Quaderi NA, Schweiger S, Gaudenz K. , et al.
Opitz G/BBB syndrome, a defect of midline development, is due to mutations in a new RING finger gene on Xp22.
Nat Genet 1997;
17 (03) 285-291
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