A Rare Case Report of 17q23.1q23.2 Microdeletion With Homozygosity of 11p11.2q13.4 in a Newborn

Sindhu Barola; Allison M. Parrill; Samaan Mahmoudzadeh; Peyman  Bizargity; Rita Verma; Sindhu Barola; Allison M. Parrill; Samaan Mahmoudzadeh; Peyman  Bizargity; Rita Verma

doi:10.7759/cureus.23290

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