Meeting Abstract
2023
·
0 citations
Novel finding in a patient with 17p13.1 deletion syndrome: a case report
Kanjee, Momen, Cinkara, Neslihan, Kahraman, Cigdem Yuce, Tatar, Abdulgani
Abstract
No abstract available for this publication.
WoS Categories
Biochemistry & Molecular Biology
Genetics & Heredity
Sustainable Development Goals
Citation
- Journal
- EUROPEAN JOURNAL OF HUMAN GENETICS
- Year
- 2023
- Volume
- 31
- Pages
- 220-220
- ISSN
- 1018-4813
- eISSN
- 1476-5438
- WoS UID
- WOS:001050507000564