Work

A de novo t (X;8)(p11.2;q24.3) demonstrating Cornelia de Lange syndrome phenotype.

Year: 2005

Type: article

Study design: Case Report

Source: PubMed

Authors: A Egemen, Z Ulger, F Ozkinay, F Gulen, O Cogulu

Institution: Ege Üniversitesi Tıp Fakültesi Hastanesi

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: W2410304251

FWCI: 0.721

Cites:

Cited by: 8

Related to: 10