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

[Study of gene mutation in 62 hemophilia A children].

Zhonghua er ke za zhi = Chinese journal of pediatrics - 2 Nov 2017

Hu Q, Liu A G, Zhang L Q, Zhang A, Wang Y Q, Wang S M, Lu Y J, Wang X

Abstract excerpt

Objective: To analyze the mutation type of FⅧ gene in children with hemophilia A and to explore the relationship among hemophilia gene mutation spectrum, gene mutation and clinical phenotype. Method: Sixty-two children with hemophilia A from Department of Pediatric Hematology, Tongji Hospital of Tongji Medical College, Huazhong University of Science and Technology between January 2015 and March 2017 were...

Read the complete abstract on PubMed

Topics

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

Share to Chromosome Inversion
Share to Codon, Nonsense
Share to Factor VIII

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Hemophilia A

Share to Infant

Share to Introns

Share to Mutation, Missense

Share to Sequence Deletion

Source

Identifiers

PMID: 29141317
DOI: 10.3760/cma.j.issn.0578-1310.2017.11.012

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Study of gene mutation in 62 hemophilia A children].PMID 29141317Read ↗

[Molecular characterization of genetic defects in hemophilia in Shanghai].Semantic proximity Read ↗

Factor 8 Gene Mutation Spectrum of 270 Patients with Hemophilia A: Identification of 36 Novel MutationsSemantic proximity Read ↗

[Correlation Analysis of FⅧGene Mutation and the Production of FⅧ Inhibitor with Severe Hemophilia A Patients in a Single Medical Center].Semantic proximity Read ↗

A strategy for the molecular diagnosis in hemophilia a in Chinese population.Semantic proximity Read ↗

Severe and moderate hemophilia A: identification of 38 new genetic alterations.Semantic proximity Read ↗

Molecular diagnosis of inversions resulting from intron 22 rearrangement of F8 gene in a patients with hemophilia A and their families and genotype-phenotype association analysisSemantic proximity Read ↗

[Application studies on the gene diagnosis and carrier detection of hemophilia A by using polymerase chain reaction-conformation sensitive gel electrophoresis].Semantic proximity Read ↗

[Analysis of Clinical Features and Gene Mutation in Children with Hereditary Coagulation Factor Deficiency].Semantic proximity Read ↗

Principles of genetic variations and molecular diseases: applications in hemophilia A.Semantic proximity Read ↗

[Molecular genetics of hemophilia A].Semantic proximity Read ↗

[Application study on inversion diagnosis of F8 gene in hemophilia A].Semantic proximity Read ↗

Genotype Hemophilia Screening Program Identified 2 Novel Variants Including a Novel Variant (c.5816-2A > G) Causing a Pathogenic Variant of the Factor 8 Gene.Semantic proximity Read ↗

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