DOI:
10.1055/s-00029027
Journal of Pediatric Genetics
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References
Robin NH, Feldman GJ, Aronson AL. , et al.
Opitz syndrome is genetically heterogeneous, with one locus on Xp22, and a second locus on 22q11.2.
Nat Genet 1995;
11 (04) 459-461
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