Novel IVS7+1G>T mutation of life-threatening congenital factor VII deficiency in neonates
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
General Medicine
Reference29 articles.
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2. Molecular analysis of the genotype-phenotype relationship in factor VII deficiency[J];Millar;Hum Genet,2000
3. Clinical phenotypes and factor VII genotype in congenital factor VII deficiency;Mariani;Thromb Haemost,2005
4. Bleeding symptoms at disease presentation and prediction of ensuing bleeding in inherited FVII deficiency;Di Minno;Thromb Haemost,2013
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1. Hereditary coagulation factor VII deficiency caused by novel compound heterozygous mutations in a Chinese pedigree: A case report;Journal of Clinical Laboratory Analysis;2022-12-26
2. Coagulation Factor VII: Genetic, Molecular, and Clinical Characteristics;Trends in Medical Sciences;2022-06-22
3. Genetics of Spontaneous Intracerebral Hemorrhage: Risk and Outcome;Frontiers in Neuroscience;2022-04-11
4. Risk and Management of Intracerebral Hemorrhage in Patients with Bleeding Disorders;Seminars in Thrombosis and Hemostasis;2022-01-06
5. Diagnosis and treatment discussion of congenital factor VII deficiency in pregnancy: A case report;World Journal of Clinical Cases;2021-07-26
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