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

Polymorphism distribution of Int13, Int22, and St14 VNTRs in a Mexican population and their application in carrier diagnosis of hemophilia A.

American journal of hematology - 1 Sept 2004

Gallegos Rafael Martínez, Aranda Herminia Benítez, Navarrete Carmen Peñaloza, Espinoza Rosenda, Gómez Fabio Salamanca, Aranda Diego Arenas

Abstract excerpt

Variable nucleotide tandem repeats (VNTR) Int13, Int22, and St14 were analyzed to determine polymorphic distribution in normal individuals from Mexico's central region and their efficacy in detecting hemophilia A carriers. Polymerase chain reaction (PCR) was carried out on 166 X chromosomes from unrelated Mexicans, and the same method was applied to detect carriers in hemophilia A families. Screening revealed the...

Read the complete abstract on PubMed

Topics

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

Share to Chromosomes, Human, X
Share to Ethnicity

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

Share to Family Health

Share to Genetic Testing

Share to Hemophilia A

Share to Heterozygote

Share to Mexico

Share to Minisatellite Repeats

Source

Identifiers

PMID: 15307098
DOI: 10.1002/ajh.20115

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

Polymorphism distribution of Int13, Int22, and St14 VNTRs in a Mexican population and their application in carrier diagnosis of hemophilia A.PMID 15307098Read ↗

The value of St14 (DXS52) VNTR analysis for genetic diagnosis of hemophilia A in Iranian population.Semantic proximity Read ↗

Rapid polymerase chain reaction analysis of St14 (DXS52) VNTR: carrier detection of hemophilia A.Semantic proximity Read ↗

[The St14 (DXS 52) VNTR in a Guangdong Han population and detection of hemophilia A carriers].Semantic proximity Read ↗

Allele frequencies of three factor VIII gene polymorphisms in Iranian populations and their application in hemophilia A carrier detection.Semantic proximity Read ↗

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

Genetic data of 15 autosomal STRs (Identifiler kit) of three Mexican Mestizo population samples from the States of Jalisco (West), Puebla (Center), and Yucatan (Southeast).Semantic proximity Read ↗

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

Frequency of intron 1 and 22 inversions of <i>factor VIII</i> gene in Mexican patients with severe hemophilia ASemantic proximity Read ↗

Allele frequencies of two polymorphisms associated with the factor IX gene in Iranian population.Semantic proximity Read ↗

PCR typing of the locus D17S30 (YNZ22 VNTR) in an Italian population sample.Semantic proximity Read ↗

Common intragenic and extragenic polymorphisms of blood coagulation factors VIII and IX are different in Chinese and Caucasian populations.Semantic proximity Read ↗

Factor VIII and IX gene polymorphisms and carrier analysis in Indian population.Semantic proximity Read ↗

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