نتائج البحث - Ladevèze, Véronique

CFTR Gene Mutations in the Egyptian Population: Current and Future Insights for Genetic Screening Strategy حسب El-Seedy, Ayman S., Shafiek, Hanaa, Kitzis, Alain, Ladevèze, Véronique

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AB174. Genetic counseling in the couple with compound heterozygous carrier based on the result of mutation effect analysis on cystic fibrosis transmembrane conductance regulator (C... حسب Permata Sari, Ariestya Indah, Farhat, Raed, Ladeveze, Véronique, Faradz, Sultana M. H., Kitzis, Alain

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Residues in the Alternative Reading Frame Tumor Suppressor that Influence its Stability and p53-Independent Activities حسب di Tommaso, Anne, Hagen, Jussara, Tompkins, Van, Muniz, Viviane, Dudakovic, Amel, Kitzis, Alain, Ladeveze, Veronique, Quelle, Dawn E.

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Influence of the Duplication of CFTR Exon 9 and Its Flanking Sequences on Diagnosis of Cystic Fibrosis Mutations حسب El-Seedy, Ayman, Dudognon, Tony, Bilan, Frédéric, Pasquet, Marie-Claude, Reboul, Marie-Pierre, Iron, Albert, Kitzis, Alain, Ladeveze, Véronique

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N1303K (c.3909C>G) Mutation and Splicing: Implication of Its c.[744-33GATT(6); 869+11C>T] Complex Allele in CFTR Exon 7 Aberrant Splicing حسب Farhat, Raëd, Puissesseau, Géraldine, El-Seedy, Ayman, Pasquet, Marie-Claude, Adolphe, Catherine, Corbani, Sandra, Megarbané, André, Kitzis, Alain, Ladeveze, Véronique

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