Your download is now in progress and you may close this window

Did you know that with a free Taylor & Francis Online account you can gain access to the following benefits?

Choose new content alerts to be informed about new research of interest to you
Easy remote access to your institution's subscriptions on any device, from any location
Save your searches and schedule alerts to send you new results
Export your search results into a .csv file to support your research

Have an account?
Login now Don't have an account?
Register for free

Login or register to access this feature

Have an account?
Login now Don't have an account?
Register for free

Choose new content alerts to be informed about new research of interest to you
Easy remote access to your institution's subscriptions on any device, from any location
Save your searches and schedule alerts to send you new results
Export your search results into a .csv file to support your research

Search in:

Advanced search

The Application of Clinical Genetics Volume 14, 2021 - Issue

Submit an article Journal homepage

Open access

836

Views

CrossRef citations to date

Altmetric

Review

The Clinical Genetics of Hemophilia B (Factor IX Deficiency)

Connie H Miller1 Division of Blood Disorders, National Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention, Atlanta, GA, USA;2 Synergy America, Inc., Duluth, GA, USACorrespondence[email protected]

https://orcid.org/0000-0002-3989-7973

Pages 445-454 | Published online: 23 Nov 2021

Cite this article
CrossMark

Full Article
Figures & data
References
Citations
Metrics
Licensing
Reprints & Permissions
View PDF PDF View EPUB EPUB

Citations (5)

Keep up to date with the latest research on this topic with citation updates for this article.

Subscribe to citation updates

Articles from other publishers (5)

Elizabeth Soffer, Karlene Coleman & Glaivy Batsuli. (2023) The impact of concurrent X chromosome anomalies on diagnosis and bleeding phenotype in children with hemophilia: A single‐institution case series. Pediatric Blood & Cancer.
Crossref

Linna Lu, Lingyu Wang, Wukang Shen, Shuai Fang, Lidong Zhao, Xuchen Hu, Linhua Yang & Gang Wang. (2023) Molecular pathogenesis of a novel Met394Thr variant causing hemophilia B . Molecular Genetics & Genomic Medicine 11:5.
Crossref

Fahrul Abdul Azis, Tutik Hardjianti, Andi Fachruddin Benyamin, Sahyuddin Saleh, Rahmawati Minhajat & Dimas Bayu. (2022) Acquired Hemophilia A in a Female: A Case Report. Open Access Macedonian Journal of Medical Sciences 10:C, pages 285-289.
Crossref

Ismail Ali Abdallah Abker, Salaheldein G. Elzaki, Salih Abdelgader Elmahdi, Jowaria Eltayeb Tayrab, Samia Mahdi Ahmed & Eltayeb Tayrab. (2022) Investigation of the Bleeding Tendency in Sudanese Female Carriers of Hemophilia B. BioMed Research International 2022, pages 1-7.
Crossref

Guomin Shen, Meng Gao, Qing Cao & Weikai Li. (2022) The Molecular Basis of FIX Deficiency in Hemophilia B. International Journal of Molecular Sciences 23:5, pages 2762.
Crossref

Related research

People also read lists articles that other readers of this article have read.

Recommended articles lists articles that we recommend and is powered by our AI driven recommendation engine.

Cited by lists all citing articles based on Crossref citations.
Articles with the Crossref icon will open in a new tab.

People also read
Recommended articles
Cited by

To cite this article:

Reference style: APA Chicago Harvard

Citation copied to clipboard

Reference styles above use APA (6th edition), Chicago (16th edition) & Harvard (10th edition)

Download citation

Download a citation file in RIS format that can be imported by citation management software including EndNote, ProCite, RefWorks and Reference Manager.

Choose format: RIS BibTex RefWorks Direct Export

Choose options: Citation Citation & abstract Citation & references