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A neonate with contiguous deletion syndrome in XP21.
Sevim U, Fatma D, Ihsan E, Gulay C, Nevin B. Sevim U, et al. Among authors: fatma d. J Pediatr Endocrinol Metab. 2011;24(11-12):1095-8. doi: 10.1515/jpem.2011.350. J Pediatr Endocrinol Metab. 2011. PMID: 22308874