Screening for hemophilia A carriers: utility of PCR-RFLP--based polymorphism analysis. - Wikidata - awgldk - TriplyDB

Screening for hemophilia A carriers: utility of PCR-RFLP--based polymorphism analysis.

Screening for hemophilia A carriers: utility of PCR-RFLP--based polymorphism analysis.

http://www.wikidata.org/entity/Q37371353

about

Identification of missense mutations in exon 16 of factor VIII gene in mild and moderate cases with hemophilia A.SNP-RFLPing 2: an updated and integrated PCR-RFLP tool for SNP genotyping.Detection of hemophilia a carriers in Azeri Turkish population of Iran: usefulness of HindIII and BclI markers.Carrier analysis for hemophilia A: ideal versus acceptable.

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Screening for hemophilia A carriers: utility of PCR-RFLP--based polymorphism analysis.

http://www.wikidata.org/entity/Q37371353

description

article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on February 2009

@en

vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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name

Screening for hemophilia A carriers: utility of PCR-RFLP--based polymorphism analysis.

@en

Screening for hemophilia A carriers: utility of PCR-RFLP--based polymorphism analysis.

@nl

type

label

Screening for hemophilia A carriers: utility of PCR-RFLP--based polymorphism analysis.

@en

Screening for hemophilia A carriers: utility of PCR-RFLP--based polymorphism analysis.

@nl

prefLabel

Screening for hemophilia A carriers: utility of PCR-RFLP--based polymorphism analysis.

@en

Screening for hemophilia A carriers: utility of PCR-RFLP--based polymorphism analysis.

@nl

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Clinical and Applied Thrombosis-Hemostasis

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Screening for hemophilia A carriers: utility of PCR-RFLP--based polymorphism analysis.

@en

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Ashutosh Kumar

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Nuzhat Husain

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Syed Tasleem Raza

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P2860

Inversions disrupting the factor VIII gene are a common cause of severe haemophilia A

Restriction fragment length polymorphisms associated with the factor VIII and factor IX genes in Polynesians.

Haemophilia A: carrier detection and prenatal diagnosis by linkage analysis using DNA polymorphism

Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants.

Investigation of factor VIII:C gene restriction fragment length polymorphisms and search for deletions in hemophiliac subjects in Algeria.

Restriction fragment length polymorphisms associated with factor VIII:C gene in Chinese.

Factor VIII gene polymorphisms in North Indian population: a consensus algorithm for carrier analysis of hemophilia A.

The prevalence study on restriction fragment length polymorphism analysis for the detection of hemophilia A carrier.

Factor VIII gene rearrangements in patients with severe haemophilia A.

Allele frequencies and molecular diagnosis in haemophilia A and B patients from Russia and from some Asian republics of the former U.S.S.R.

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78-83

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scholarly article

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10.1177/1076029607305105

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1

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2009-02-01T00:00:00Z

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