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Results: 1-2 |
Results: 2
A dimorphic 4-bp repeat in the cystic fibrosis gene is in absolute linkage disequilibrium with the delta F508 mutation: implications for prenatal diagnosis and mutation origin.
Authors: Chehab, Farid F. Johnson, John Louie, Elaine Goossens, Michel Kawasaki, Ernie Erlich, Henry
Citation: F. Chehab, Farid et al., A dimorphic 4-bp repeat in the cystic fibrosis gene is in absolute linkage disequilibrium with the delta F508 mutation: implications for prenatal diagnosis and mutation origin., American journal of human genetics , 48-I(2), 1991, pp. 223-226
Screening for non-delta F508 mutations in five exons of the cystic fibrosis transmembrane conductance regulator (CFTR) gene in Italy.
Authors: Devoto, Marcella Ronchetto, Patrizia Fanen, Pascale Orriols, Juan Jose Telleria Romeo, Giovanni Goossens, Michel Ferrari, Maurizio Magnani, Carmelina Seia, Manuela Cremonesi, Laura
Citation: Devoto, Marcella et al., Screening for non-delta F508 mutations in five exons of the cystic fibrosis transmembrane conductance regulator (CFTR) gene in Italy., American journal of human genetics , 48-II(6), 1991, pp. 1127-1132
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