Resolving fetal hydrops – A rare entity
Author:
Funder
Indian Council of Medical Research
Publisher
Elsevier BV
Subject
Genetics (clinical),Genetics,General Medicine
Reference10 articles.
1. A recessive truncating variant in thrombospondin-1 domain containing protein 1 gene THSD1 is the underlying cause of nonimmune hydrops fetalis, congenital cardiac defects, and haemangiomas in four patients from a consanguineous family;Abdelrahman;Am. J. Med. Genet.,2018
2. Manifestations of thrombospondin type-1 domain-containing protein 1 gene mutation in an extremely premature infant with nonimmune hydrops fetalis;Al Rawi;Am. J. Med. Genet.,2021
3. THSD1 preserves vascular integrity and protects against intraplaque haemorrhaging in ApoE-/- mice;Haasdijk;Cardiovasc. Res.,2016
4. A systematic review of monogenic etiologies of nonimmune hydrops fetalis;Quinn;Genet. Med.,2021
5. The intracranial aneurysm gene THSD1 connects endosome dynamics to nascent focal adhesion assembly;Rui;Cell. Physiol. Biochem.,2017
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