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Salmo Raskin

Biographic Data

ID3715553
NAMESalmo Raskin
GIVEN NAMESSalmo
FAMILY NAMERaskin
SIGNATURERASKIN S
AFFILIATIONSUniversidade Federal do Paraná
ORCID0000-0002-7191-0592
VERIFIEDYes
TOTAL WORKS3
TOTAL CITATIONS2
WORKS AS AUTHOR3
WORKS AS EDITOR0
FIRST PUBLICATION YEAR1995
LATEST PUBLICATION YEAR2007
H-INDEX1
  • Cystic Fibrosis Gene Variability in Two Southern Brazilian Amerindian Populations

    Salmo Raskin, M Luiza Petzl‐erler et al.•ARTICLE•Human Biology•2007•References: 2

    The frequencies of the deltaF508 deletion, the most common cystic fibrosis mutation in Europeans and European-derived populations, and the XV2C and KM19 restriction fragment length polymorphisms that are tightly linked to the CFTR locus vary among populations. To determine the distribution of these extragenic markers and of the deltaF508 mutation, we analyzed 326 chromosomes of individuals from two South American Indian populations, the Guarani a…

  • CFTR Molecular Analysis Reveals Infrequent Allele Frequencies in Nine Cystic Fibrosis Patients from Sao Paulo State, Brazil

    Eny Maria Goloni-Bertollo, Eny Maria Goloni‐Bertollo et al.•ARTICLE•Human Biology•2003

    Although cystic fibrosis (CF) is the most common autosomal recessive disorder in whites, it is thought to be relatively rare or, alternatively, underdiagnosed in Latin America. In Brazil, different groups have shown a DF508 mutation frequency ranging from 30.7% to 50.8%. Such variation may be explained by the ethnic differences observed in this country, which is genetically very heterogeneous. We describe the molecular analysis for 32 mutations o…

  • Ética e genética

    Open Access•Salmo Raskin•ARTICLE•Educar em Revista•1995•Cited by: 2

    A ousadia da ciencia chegou a producao de seres humanos. O mundo e o Brasil discutem a necessidade de se criar codigos de etica para acompanhar o desenvolvimento da ciencia no que diz respeito a reproducao humana e manipulacao genetica. A diversidade da especie podera ser comprometida

  • Ética e genética

    Open Access•Salmo Raskin•ARTICLE•Educar em Revista•1995•Cited by: 2

    A ousadia da ciencia chegou a producao de seres humanos. O mundo e o Brasil discutem a necessidade de se criar codigos de etica para acompanhar o desenvolvimento da ciencia no que diz respeito a reproducao humana e manipulacao genetica. A diversidade da especie podera ser comprometida

  • Ética e genética

    Open Access•Salmo Raskin•ARTICLE•Educar em Revista•1995•Cited by: 2

    A ousadia da ciencia chegou a producao de seres humanos. O mundo e o Brasil discutem a necessidade de se criar codigos de etica para acompanhar o desenvolvimento da ciencia no que diz respeito a reproducao humana e manipulacao genetica. A diversidade da especie podera ser comprometida

  • CFTR Molecular Analysis Reveals Infrequent Allele Frequencies in Nine Cystic Fibrosis Patients from Sao Paulo State, Brazil

    Eny Maria Goloni-Bertollo, Eny Maria Goloni‐Bertollo et al.•ARTICLE•Human Biology•2003

    Although cystic fibrosis (CF) is the most common autosomal recessive disorder in whites, it is thought to be relatively rare or, alternatively, underdiagnosed in Latin America. In Brazil, different groups have shown a DF508 mutation frequency ranging from 30.7% to 50.8%. Such variation may be explained by the ethnic differences observed in this country, which is genetically very heterogeneous. We describe the molecular analysis for 32 mutations o…

  • Cystic Fibrosis Gene Variability in Two Southern Brazilian Amerindian Populations

    Salmo Raskin, M Luiza Petzl‐erler et al.•ARTICLE•Human Biology•2007•References: 2

    The frequencies of the deltaF508 deletion, the most common cystic fibrosis mutation in Europeans and European-derived populations, and the XV2C and KM19 restriction fragment length polymorphisms that are tightly linked to the CFTR locus vary among populations. To determine the distribution of these extragenic markers and of the deltaF508 mutation, we analyzed 326 chromosomes of individuals from two South American Indian populations, the Guarani a…

Allele (2 works) · Allele frequency (2 works) · Biology (2 works) · Congenital Ear and Nasal Anomalies (2 works) · Cystic fibrosis (2 works) · Cystic Fibrosis Research Advances (2 works) · Gene (2 works) · Genetics (2 works) · Genetics (2 works) · Mutation (2 works)

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