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

Value of DNA analysis with multiple DNA probes for the detection of hemophilia A carriers.

Pediatric hematology and oncology - 1 Jan 2000

Kemahli S, Goldman E, McCraw A, Jenkins V, Kernoff P B

Abstract excerpt

Detection of hemophilia carriers is an important issue and should be addressed with great care. The allelic frequencies of three intragenic probes (Bcl I for probe p114.12, Xba I for probe p482.6, and Bgl I for probe C) and one linked probe (Bgl II for probe DX 13) are reported, together with their diagnostic yield singly and in combination. In this series, 725 individuals (405 females) in 156 families were...

Read the complete abstract on PubMed

Topics

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

Share to Alleles
Share to DNA
Share to DNA Probes

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

Share to Gene Frequency

Share to Genetic Carrier Screening

Share to Genetic Linkage

Share to Hemophilia A

Share to Prenatal Diagnosis

Source

Identifiers

PMID: 8155501
DOI: 10.3109/08880019409141901

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

Value of DNA analysis with multiple DNA probes for the detection of hemophilia A carriers.PMID 8155501Read ↗

Carrier detection and prenatal diagnosis in 98 families of haemophilia A by linkage analysis and direct detection of mutations.Semantic proximity Read ↗

Factor VIII gene mutations and RFLP analysis in hemophilia A.Semantic proximity Read ↗

Carrier detection of hemophilia A in a Mexican population by two Bcl I polymorphisms.Semantic proximity Read ↗

Evaluation of DNA-based diagnosis for haemophilia A.Semantic proximity Read ↗

Carrier detection for prenatal diagnosis of hemophilia A in Italian families.Semantic proximity Read ↗

Detection of carriers of haemophilia A: use of bioassays and restriction fragment length polymorphisms (RFLP).Semantic proximity Read ↗

Carrier detection for hemophilia B: evaluation of multiple polymorphic sites.Semantic proximity Read ↗

DNA analysis of haemophilia A families from southern France. Experience of a hospital laboratory.Semantic proximity Read ↗

Analysis of five polymorphic DNA markers for indirect genetic diagnosis of haemophilia A in the Brazilian population.Semantic proximity Read ↗

Genomic diagnosis of haemophilia A and B in the German Democratic Republic.Semantic proximity Read ↗

Carrier detection and prenatal diagnosis in families with haemophilia.Semantic proximity Read ↗

Analysis of Factor VIII polymorphic markers as a means for carrier detection in Brazilian families with haemophilia A.Semantic proximity Read ↗

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