Kapak Resmi

CLINICAL CASE OF CHROMOSOME 22Q11.2 DELETION SYNDROME (DI-GEORGIE SYNDROME)

A clinical case of orphan genetic pathology - Di Georgi syndrome in a child in the neonatal period is presented. The complexity of timely diagnosis of this complication is demonstrated.

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Detaylı Bibliyografya
Asıl Yazarlar:	Ирина Анатольевна Никитина (Yazar), Елена Глебовна Цой (Yazar), Светлана Владимировна Цигельник (Yazar), Вадим Гельевич Мозес (Yazar), Светлана Ивановна Елгина (Yazar), Елена Владимировна Рудаева (Yazar)
Materyal Türü:	Kitap
Baskı/Yayın Bilgisi:	The Publishing House Medicine and Enlightenment, 2020-02-01T00:00:00Z.
Konular:	article
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Etiketler:	Etiketle Etiket eklenmemiş, İlk siz ekleyin!

Diğer Bilgiler
Özet:	A clinical case of orphan genetic pathology - Di Georgi syndrome in a child in the neonatal period is presented. The complexity of timely diagnosis of this complication is demonstrated.
Diğer Bilgileri:	1991-010X 2542-0968