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 framework for genetic service provision for haemophilia and other inherited bleeding disorders

1 Mar 2005

Abstract excerpt

This framework document offers guidance to patients, doctors, nurses, laboratory scientists, funders and hospitals on the provision of clinical and laboratory genetic services for haemophilia. With recent advances in molecular laboratory techniques it is now possible to give the vast majority of individual patients and family members very reliable genetic information. To enable these genetic data to be used for...

Read the complete abstract on PubMed

Topics

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

Share to Hemophilia Treatment and Research

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 15810917
DOI: 10.1111/j.1365-2516.2005.01070.x

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A framework for genetic service provision for haemophilia and other inherited bleeding disordersPMID 15810917Read ↗

The molecular analysis of haemophilia B: a guideline from the UK haemophilia centre doctors' organization haemophilia genetics laboratory network.Semantic proximity Read ↗

The molecular analysis of haemophilia A: a guideline from the UK haemophilia centre doctors' organization haemophilia genetics laboratory network.Semantic proximity Read ↗

Genetic diagnosis of haemophilia and other inherited bleeding disordersSemantic proximity Read ↗

Insights into the Molecular Genetic of Hemophilia A and Hemophilia B: The Relevance of Genetic Testing in Routine Clinical Practice.Semantic proximity Read ↗

EMQN Best Practice Guidelines for molecular and haematology methods for carrier identification and prenatal diagnosis of the haemoglobinopathies.Semantic proximity Read ↗

Consent and confidentiality in clinical genetic practice: guidance on genetic testing and sharing genetic informationSemantic proximity Read ↗

Role of molecular genetics in hemophilia: from diagnosis to therapy.Semantic proximity Read ↗

Management of rare inherited bleeding disorders: Proposals of the French Reference Centre on Haemophilia and Rare Coagulation Disorders.Semantic proximity Read ↗

Updated Australian consensus statement on management of inherited bleeding disorders in pregnancySemantic proximity Read ↗

Genetic services available for counselling and prenatal diagnosis of haemophilia.Semantic proximity Read ↗

Proactive systematic hemophilia carrier screening: a step toward gender equity in hemophilia careSemantic proximity Read ↗

Recommendations for reporting results of diagnostic genetic testing (biochemical, cytogenetic and molecular genetic)Semantic proximity Read ↗

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