Response to “characteristics of 2p15‐p16.1 microdeletion syndrome: review and description of two additional patients”

Publisher: John Wiley & Sons Inc

E-ISSN: 1741-4520|55|4|191-192

ISSN: 0914-3505

Source: CONGENITAL ANOMALIES, Vol.55, Iss.4, 2015-11, pp. : 191-192

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Abstract