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Kada Krabchi

Showing results (1-10 of 9) with videos related to

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Methods in Molecular Biology (Clifton, N.J.)|July 25, 2006
New rapid multicolor PRINS protocolJu Yan, Macoura Gadji, Kada Krabchi, et al.
Methods in Molecular Biology (Clifton, N.J.)|July 25, 2006
Dual-color PRINS for in situ detection of fetal cells in maternal bloodKada Krabchi, Macoura Gadji, Ju Yan, et al.
Methods in Molecular Biology (Clifton, N.J.)|April 22, 2008
Application of multi-PRINS to simultaneously identify chromosomes 18, X, and Y in prenatal diagnosisMacoura Gadji, Kada Krabchi, Ju Yan, et al.
Medecine Sciences : M/S|May 5, 2004
[From the conception of the PRINS to its coronation]Kada Krabchi, Josée Lavoie, Philippe Coullin, et al.
Medecine Sciences : M/S|March 11, 2006
[Dominant negative activity of mutated p53 proteins]Walid Dridi, Kada Krabchi, Macoura Gadji, et al.
Prenatal Diagnosis|December 24, 2005
Quantification of fetal nucleated cells in maternal blood of pregnant women with a male trisomy 21 fetus using molecular cytogenetic techniquesKada Krabchi, Macoura Gadji, Oumar Samassekou, et al.
American Journal of Medical Genetics. Part A|January 30, 2016
Three new cases of terminal deletion of the long arm of chromosome 7 and literature review to correlate genotype and phenotype manifestationsSeemi Ayub, Macoura Gadji, Kada Krabchi, et al.
Journal of Biomedicine & Biotechnology|April 17, 2012
Efficiency of manual scanning in recovering rare cellular events identified by fluorescence in situ hybridization: simulation of the detection of fetal cells in maternal bloodAhmed Emad, Seemi Ayub, Oumar Samassékou, et al.
American Journal of Medical Genetics. Part A|June 17, 2008
Partial trisomy of chromosome 22 resulting from a supernumerary marker chromosome 22 in a child with features of cat eye syndromeValérie Bélien, Marion Gérard-Blanluet, Stéphane Serero, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Methods in Molecular Biology (Clifton, N.J.)|July 25, 2006
New rapid multicolor PRINS protocolJu Yan, Macoura Gadji, Kada Krabchi, et al.
Methods in Molecular Biology (Clifton, N.J.)|July 25, 2006
Dual-color PRINS for in situ detection of fetal cells in maternal bloodKada Krabchi, Macoura Gadji, Ju Yan, et al.
Methods in Molecular Biology (Clifton, N.J.)|April 22, 2008
Application of multi-PRINS to simultaneously identify chromosomes 18, X, and Y in prenatal diagnosisMacoura Gadji, Kada Krabchi, Ju Yan, et al.
Medecine Sciences : M/S|May 5, 2004
[From the conception of the PRINS to its coronation]Kada Krabchi, Josée Lavoie, Philippe Coullin, et al.
Medecine Sciences : M/S|March 11, 2006
[Dominant negative activity of mutated p53 proteins]Walid Dridi, Kada Krabchi, Macoura Gadji, et al.
Prenatal Diagnosis|December 24, 2005
Quantification of fetal nucleated cells in maternal blood of pregnant women with a male trisomy 21 fetus using molecular cytogenetic techniquesKada Krabchi, Macoura Gadji, Oumar Samassekou, et al.
American Journal of Medical Genetics. Part A|January 30, 2016
Three new cases of terminal deletion of the long arm of chromosome 7 and literature review to correlate genotype and phenotype manifestationsSeemi Ayub, Macoura Gadji, Kada Krabchi, et al.
Journal of Biomedicine & Biotechnology|April 17, 2012
Efficiency of manual scanning in recovering rare cellular events identified by fluorescence in situ hybridization: simulation of the detection of fetal cells in maternal bloodAhmed Emad, Seemi Ayub, Oumar Samassékou, et al.
American Journal of Medical Genetics. Part A|June 17, 2008
Partial trisomy of chromosome 22 resulting from a supernumerary marker chromosome 22 in a child with features of cat eye syndromeValérie Bélien, Marion Gérard-Blanluet, Stéphane Serero, et al.
Pageof 1