Work

3q13.31 deletion syndrome in a patient with autistic features and global developmental delay

Year: 2021

Type: article

Study design: Case Report

Authors: Aurora Arghir, Sorina Mihaela Papuc, Alina Erbescu, G. Gaina, Carmen Burloiu, Magdalena Budișteanu

Language: English

Topic: Genomic variations and chromosomal abnormalities

Subfield: Genetics

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

OpenAlex ID: W3173459495

FWCI:

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Related to: 10