Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

[A family with hereditary coagulation factor deficiency].

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics - 1 Feb 2013

Zhang Teng-long, Liu Bo, Zhang Peng, Xing Xiu-hua, Meng Yue-sheng, Lan Qiao-ling

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Factor VII Deficiency
Share to Pedigree
Share to Phenotype

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 23450497
DOI: 10.3760/cma.j.issn.1003-9406.2013.01.031

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[A family with hereditary coagulation factor deficiency].PMID 23450497Read ↗

[Analysis of clinical features and genotype in an inherited coagulation factor Ⅶ deficiency pedigree].Semantic proximity Read ↗

[Analysis of the molecular pathogenesis and clinical phenotypes of 10 patients with inherited coagulation factor Ⅺ deficiency].Semantic proximity Read ↗

[Gene diagnosis of a family with coagulation factor ⅩⅢ deficiency caused by large deletion of F13A1 gene].Semantic proximity Read ↗

[Congenital coagulopathies: clinical manifestation and molecular mechanism].Semantic proximity Read ↗

[Phenotypic and genetic analysis of a pedigree with inherited antithrombin deficiency].Semantic proximity Read ↗

[Molecular anomalies of coagulation inhibitors].Semantic proximity Read ↗

[A family with hereditary FⅪ deficiency caused by compound heterozygous mutation].Semantic proximity Read ↗

[Hereditary thrombophilia: prospects].Semantic proximity Read ↗

[Two novel factor V gene mutations associated with congenital coagulation factor V deficiency, study of one pedigree].Semantic proximity Read ↗

[Molecular basis of hereditary thrombophilia].Semantic proximity Read ↗

[Thrombophilia--often a case of genetic susceptibility. Thrombosis ABC, 6: Protein C deficiency].Semantic proximity Read ↗

[Structural and functional analysis of mutant blood coagulation and fibrinolytic factors].Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.