Search Results - Krabchi, Kada

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  1. 1
    Three new cases of terminal deletion of the long arm of chromosome 7 and literature review to correlate genotype and phenotype manifestations

    Three new cases of terminal deletion of the long arm of chromosome 7 and literature review to correlate genotype and phenotype manifestations by Ayub, Seemi, Gadji, Macoura, Krabchi, Kada, Côté, Sylvie, Gekas, Jean, Maranda, Bruno, Drouin, Régen

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  2. 2
    Efficiency of Manual Scanning in Recovering Rare Cellular Events Identified by Fluorescence In Situ Hybridization: Simulation of the Detection of Fetal Cells in Maternal Blood

    Efficiency of Manual Scanning in Recovering Rare Cellular Events Identified by Fluorescence In Situ Hybridization: Simulation of the Detection of Fetal Cells in Maternal Blood by Kilpatrick, Michael W., Krabchi, Kada, Drouin, Régen, Hemmings, Francis, Lamoureux, Josée, Ntwari, Aimé, Gadji, Macoura, Grégoire, Marie-Chantal, Samassékou, Oumar, Ayub, Seemi, Emad, Ahmed, Tafas, Triantafyllos

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  3. 3
    Prenatal diagnosis and molecular characterization of two constitutional rings derived from one chromosome 22

    Prenatal diagnosis and molecular characterization of two constitutional rings derived from one chromosome 22 by Gadji, Macoura, Krabchi, Kada, Langis, Paul, Aboura, Azeddine, Périgny, Martine, Côté, Stéphanie, Ferland, Mélissa, Drouin, Régen

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  4. 4
    Quantification of fetal nucleated cells in maternal blood of pregnant women with a male trisomy 21 fetus using molecular cytogenetic techniques

    Quantification of fetal nucleated cells in maternal blood of pregnant women with a male trisomy 21 fetus using molecular cytogenetic techniques by Krabchi, Kada, Gadji, Macoura, Samassekou, Oumar, Grégoire, Marie-Chantal, Forest, Jean-Claude, Drouin, Régen

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  5. 5
    Partial trisomy of chromosome 22 resulting from a supernumerary marker chromosome 22 in a child with features of cat eye syndrome

    Partial trisomy of chromosome 22 resulting from a supernumerary marker chromosome 22 in a child with features of cat eye syndrome by Bélien, Valérie, Gérard‐Blanluet, Marion, Serero, Stéphane, Le Dû, Nathalie, Baumann, Clarisse, Jacquemont, Marie‐Line, Dupont, Céline, Krabchi, Kada, Drunat, Séverine, Elbez, Annie, Janaud, Jean‐Claude, Benzacken, Brigitte, Verloes, Alain, Tabet, Anne‐Claude, Aboura, Azzedine

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  6. 6
    Efficiency of Manual Scanning in Recovering Rare Cellular Events Identified by Fluorescence In Situ Hybridization : Simulation of the Detection of Fetal Cells in Maternal Blood

    Efficiency of Manual Scanning in Recovering Rare Cellular Events Identified by Fluorescence In Situ Hybridization : Simulation of the Detection of Fetal Cells in Maternal Blood by Ayub, Seemi, Emad, Ahmed, Samassékou, Oumar, Grégoire, Marie-Chantal, Gadji, Macoura, Ntwari, Aimé, Lamoureux, Josée, Hemmings, Francis, Tafas, Triantafyllos, Kilpatrick, Michael W., Krabchi, Kada, Drouin, Régen

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  7. 7
    Prenatal diagnosis and molecular characterization of two constitutional rings derived from one chromosome 22

    Prenatal diagnosis and molecular characterization of two constitutional rings derived from one chromosome 22 by Gadji, Macoura, Krabchi, Kada, Langis, Paul, Aboura, Azeddine, Périgny, Martine, Côté, Stéphanie, Ferland, Mélissa, Drouin, Régen

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  8. 8
    Partial trisomy of chromosome 22 resulting from a supernumerary marker chromosome 22 in a child with features of cat eye syndrome

    Partial trisomy of chromosome 22 resulting from a supernumerary marker chromosome 22 in a child with features of cat eye syndrome by Bélien, Valérie, Gérard-Blanluet, Marion, Serero, Stéphane, Le Dû, Nathalie, Baumann, Clarisse, Jacquemont, Marie-Line, Dupont, Céline, Krabchi, Kada, Drunat, Séverine, Elbez, Annie, Janaud, Jean-Claude, Benzacken, Brigitte, Verloes, Alain, Tabet, Anne-Claude, Aboura, Azzedine

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