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dc.contributor.authorCarrillo Perez MD
dc.contributor.authorFragoso Herrera R
dc.contributor.authorCisneros Vega B
dc.contributor.authorAmparo Esparza M
dc.contributor.authorCantu JM
dc.contributor.authorMontanez Ojeda C
dc.identifier.issn0188-4409; 0188-4409
dc.description.abstractThe frequency of alleles, intragenic (intron 18) and extragenic (DXS52) Bcl I RFLPs was investigated in a sample of the Mexican population. Altogether 33 X chromosomes at R8c locus and 30 at DXS52 locus were studied. The allele frequencies found at the F8c locus were similar to those reported in the majority of other populations. The observed heterozygosity for the intragenic and extragenic markers were 0.57 and 0.64, respectively. By using these two RFLPs 15 females at risk in five independent families with hemophilia A were investigated; ten of them could be identified and five excluded as carriers.
dc.titleCarrier detection of hemophilia A in a Mexican population by two Bcl I polymorphisms.
dc.typeJournal Article
dc.relation.ispartofjournalArchives of Medical Research
dc.subject.keywordIndex Medicus;Alleles;Female;Gene Frequency;Hemophilia A/ep [Epidemiology];Hemophilia A/ge [Genetics];Heterozygote Detection;Humans;Male;Mexico/ep [Epidemiology];Pedigree;Polymorphism, Restriction Fragment Length
dc.contributor.affiliationCarrillo Perez,M D. Division de Genetica, Universidad de Guadalajara, IMSS, Jalisco, Mexico.
dc.description.noteRecord Owner: From MEDLINE, a database of the U.S. National Library of Medicine.; Status: MEDLINE; Publishing Model: Journal available in: Print Citation processed from: Print; NLM Journal Code: bic, 9312706; Entry Date: 19940208
Appears in Collections:Producción científica UdeG

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