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

New approaches to the genetic study of bleeding diathesis in our center: from sanger to next-generation sequencing.

Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis - 1 Jan 2022

Corrales Irene

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 Disease Susceptibility
Share to High-Throughput Nucleotide Sequencing
Share to Mutation
Share to Sequence Analysis, DNA

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 35088770
DOI: 10.1097/MBC.0000000000001107

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

New approaches to the genetic study of bleeding diathesis in our center: from sanger to next-generation sequencing.PMID 35088770Read ↗

Curated disease‐causing genes for bleeding, thrombotic, and platelet disorders: Communication from the SSC of the ISTHSemantic proximity Read ↗

Hemostatic phenotypes and genetic disordersSemantic proximity Read ↗

Genetic sequence analysis of inherited bleeding diseasesSemantic proximity Read ↗

The role of genetics in the diagnosis and treatment of haemorrhagic diathesis: a historical perspective.Semantic proximity Read ↗

Molecular Diagnosis of Inherited Coagulation and Bleeding DisordersSemantic proximity Read ↗

High-throughput sequencing approaches for diagnosing hereditary bleeding and platelet disorders.Semantic proximity Read ↗

Molecular testing for disorders of hemostasis.Semantic proximity Read ↗

Genomic approaches to bleeding disorders.Semantic proximity Read ↗

A high-throughput sequencing test for diagnosing inherited bleeding, thrombotic, and platelet disorders.Semantic proximity Read ↗

Diagnosis of inherited bleeding disorders in the genomic era.Semantic proximity Read ↗

Laboratory testing for heritable thrombophilia: impact on clinical management of thrombotic disease annotation.Semantic proximity Read ↗

Variant discovery in patients with Mendelian vascular anomalies by next-generation sequencing and their use in patient clinical management.Semantic proximity Read ↗

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