Diagnosis of 9q22.3 microdeletion syndrome in utero following identification of craniosynostosis, overgrowth, and skeletal anomalies

Publisher: John Wiley & Sons Inc

E-ISSN: 1552-4833|167|4|862-865

ISSN: 1552-4825

Source: American Journal Of Medical Genetics Part A, Vol.167, Iss.4, 2015-04, pp. : 862-865

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