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

Analysis of Phenotype and Genotypein an Inherited Coagulation Factor VII Deficiency Pedigree.

Clinical laboratory - 1 Dec 2019

Li Min, Jin Yanhui, Wang Mingshan, Ding Hongxiang

Abstract excerpt

BACKGROUND: To identify potential mutations and analyze the phenotype in an inherited factor VII (FVII) deficiency pedigree. METHODS: Prothrombin time (PT), activated partial thromboplastin time (APTT), fibrinogen, FVII activity (FVII:C), FVII antigen (FVII:Ag) and other coagulant parameters of the proband and family members were measured. Calibrated automated thrombin generation measurements were used to detect...

Read the complete abstract on PubMed

Topics

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

Share to Antigens
Share to Asian People
Share to China

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Factor VII

Share to Factor VII Deficiency

Share to Heterozygote

Share to Partial Thromboplastin Time

Share to Prothrombin Time

Source

Identifiers

PMID: 31850724
DOI: 10.7754/Clin.Lab.2019.190710

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Analysis of Phenotype and Genotypein an Inherited Coagulation Factor VII Deficiency Pedigree.PMID 31850724Read ↗

[Molecular analysis of two pedigrees with inherited coagulation factor VII deficiency].Semantic proximity Read ↗

Analysis of phenotype and genotype of a family with hereditary coagulation factor V deficiency caused by the compound heterozygous mutations.Semantic proximity Read ↗

[Genotype and phenotype analysis of congenital coagulator factor VII deficiency in four Chinese pedigrees].Semantic proximity Read ↗

Genetic analysis of a pedigree with hereditary coagulation factor XII deficiencySemantic proximity Read ↗

[Phenotype and Genotype Analysis in Two Pedigrees with Hereditary Coagulation Factor Ⅺ Deficiency].Semantic proximity Read ↗

[Identification of genetic defects in a Chinese pedigree with factor XIII deficiency: case report and literature review].Semantic proximity Read ↗

[Genetic analysis of a Chinese pedigree affected with Hereditary coagulation factor Ⅴ deficiency due to compound heterozygous variants IVS24+3A>T and p.Asp2222Gly].Semantic proximity Read ↗

[Gene analysis of a combined inherited factor VII and factor X deficiency pedigree].Semantic proximity Read ↗

[Analysis of Phenotype and Genotype of A Family with Hereditary Coagulation Factor Ⅴ Deficiency Caused by A Compound Heterozygous Mutation].Semantic proximity Read ↗

Hereditary coagulation factor VII deficiency caused by novel compound heterozygous mutations in a Chinese pedigree: A case report.Semantic proximity Read ↗

[Severe hereditary coagulation factor V deficiency caused by two novel heterozygous mutations].Semantic proximity Read ↗

Recurrent Founder Variant in Inherited FVII Deficiency: Molecular Spectrum Analysis in Southeast China Recurrent Founder Variant in Inherited FVII Deficiency: Molecular Spectrum Analysis in Southeast ChinaSemantic proximity Read ↗

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