Work

Prenatal diagnosis and genetic counselling of a rare de-novo 12p13.33p13.32 deletion and 15q26.2q26.3 duplication in a Chinese family

Year: 2026

Type: article

Study design: Case Report

Source: Psychiatric Genetics

DOI: 10.1097/ypg.0000000000000412

Authors: Zhenzhen Zhang, Wei Wang, Jin Xiong, Qi Xia

Institutions: Hubei University of Medicine, Hubei Provincial Women and Children's Hospital

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: W7128407887

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