Literature DB >> 19842127

Inverse shifting PCR based prenatal diagnosis of hemophilia-causative inversions involving int22h and int1h hotspots from chorionic villus samples.

Claudia P Radic1, Liliana C Rossetti, Johanna R Zuccoli, Martín M Abelleyro, Irene B Larripa, Carlos D De Brasi.   

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Year:  2009        PMID： 19842127     DOI： 10.1002/pd.2393

Source DB:  PubMed          Journal:  Prenat Diagn        ISSN： 0197-3851            Impact factor:   3.050


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  3 in total

Review 1.  Genetic testing in bleeding disorders.

Authors:  C de Brasi; O El-Maarri; D J Perry; J Oldenburg; B Pezeshkpoor; A Goodeve
Journal:  Haemophilia       Date:  2014-05       Impact factor: 4.287

Review 2.  Eighteen years of molecular genotyping the hemophilia inversion hotspot: from southern blot to inverse shifting-PCR.

Authors:  Liliana C Rossetti; Claudia P Radic; Miguel M Abelleyro; Irene B Larripa; Carlos D De Brasi
Journal:  Int J Mol Sci       Date:  2011-10-24       Impact factor: 5.923

3.  5meCpG epigenetic marks neighboring a primate-conserved core promoter short tandem repeat indicate X-chromosome inactivation.

Authors:  Filipe Brum Machado; Fabricio Brum Machado; Milena Amendro Faria; Viviane Lamim Lovatel; Antonio Francisco Alves da Silva; Claudia Pamela Radic; Carlos Daniel De Brasi; Álvaro Fabricio Lopes Rios; Susana Marina Chuva de Sousa Lopes; Leonardo Serafim da Silveira; Carlos Ramon Ruiz-Miranda; Ester Silveira Ramos; Enrique Medina-Acosta
Journal:  PLoS One       Date:  2014-07-31       Impact factor: 3.240
  3 in total

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