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

Unexpected haemophilia despite pre-natal testing - a combined haemophilia A and haemophilia B family.

British journal of haematology - 1 Oct 2017

Roy Noémi B A, Curry Nicola, Keeling David

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 Amino Acid Substitution
Share to Factor IX
Share to Factor VIII
Share to Family

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

Share to Hemophilia A

Share to Hemophilia B

Share to Pedigree

Share to Prenatal Diagnosis

Source

Identifiers

PMID: 28677841
DOI: 10.1111/bjh.14840

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 23 Oct 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

Unexpected haemophilia despite pre-natal testing - a combined haemophilia A and haemophilia B family.PMID 28677841Read ↗

Prenatal diagnosis in haemophilia A: experience of the genetic diagnostic laboratory.Semantic proximity Read ↗

A new strategy for carrier and prenatal diagnosis and molecular studies in haemophilia B.Semantic proximity Read ↗

Genetic causes of haemophilia in women and girls.Semantic proximity Read ↗

Clinical and molecular characteristics of hemophilia A affected individuals and carriers: A 24 years experience from three centers.Semantic proximity Read ↗

The diagnosis and evaluation of women and girls with hemophilia and hemophilia carriers: guidance from the SSC of the ISTH.Semantic proximity Read ↗

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 ↗

Puzzling outcome of the nationwide genetic survey of severe/moderate female haemophilia B in Poland.Semantic proximity Read ↗

Clinical guidelines for testing for heritable thrombophilia.Semantic proximity Read ↗

Hereditary Thrombotic Thrombocytopenic Purpura in a 9-Month-old: Diagnosing and Managing an Ultra-rare Disorder.Semantic proximity Read ↗

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

Six molecular patterns leading to hemophilia A phenotype in 18 females from Poland.Semantic proximity Read ↗

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