DOI:
10.1055/s-00029027
Journal of Pediatric Genetics
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References
Weegerink NJ, Swinnen FK, Vanakker OM, Casselman JW, Dhooge IJ.
Phenotype of a Belgian family with 6p25 deletion syndrome.
Ann Otol Rhinol Laryngol 2016;
125 (09) 734-745
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