DOI:
10.1055/s-00029027
Journal of Pediatric Genetics
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References
Delahaye A, Toutain A, Aboura A. , et al.
Chromosome 22q13.3 deletion syndrome with a de novo interstitial 22q13.3 cryptic deletion disrupting SHANK3.
Eur J Med Genet 2009;
52 (05) 328-332
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