2q13 microdeletion syndrome: Report on a newborn with additional features expanding the phenotype

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3 Citazioni (Scopus)

Abstract

We describe an additional newborn with craniofacial dysmorphisms, congenital heart disease, hypotonia, and a 2q13 deletion of 1.7 Mb. The clinical and genomic findings observed are consistent with the diagnosis of 2q13 microdeletion syndrome.
Lingua originaleEnglish
pagine (da-a)1-5
Numero di pagine5
RivistaClinical Case Reports
Volume9
Stato di pubblicazionePublished - 2021

All Science Journal Classification (ASJC) codes

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