Please use this identifier to cite or link to this item:
https://hdl.handle.net/11499/56860
Title: | A case report of Hennekam syndrome with a mutation in the CCBE1 gene | Authors: | Durak, T. Karaer, D. Karaer, K. |
Keywords: | calcium binding protein CCBE1 protein, human tumor suppressor protein case report craniofacial malformation human intestine lymphangiectasia lymphedema mutation Calcium-Binding Proteins Craniofacial Abnormalities Hennekam lymphangiectasia lymphedema syndrome Humans Lymphangiectasis, Intestinal Lymphedema Mutation Tumor Suppressor Proteins |
Publisher: | Lippincott Williams and Wilkins | Abstract: | [No abstract available] | URI: | https://doi.org/10.1097/MCD.0000000000000488 https://hdl.handle.net/11499/56860 |
ISSN: | 0962-8827 |
Appears in Collections: | PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection Tıp Fakültesi Koleksiyonu WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection |
Show full item record
CORE Recommender
SCOPUSTM
Citations
1
checked on Sep 8, 2025
WEB OF SCIENCETM
Citations
1
checked on Aug 26, 2025
Page view(s)
128
checked on Sep 8, 2025
Google ScholarTM
Check
Altmetric
Items in GCRIS Repository are protected by copyright, with all rights reserved, unless otherwise indicated.