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V Cacheux

Showing results (11-20 of 28) with videos related to

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American Journal of Medical Genetics|April 6, 1999
De novo inverted duplication 9p21pter involving telomeric repeated sequencesD Sanlaville, C Baumann, J M Lapierre, et al.
Fetal Diagnosis and Therapy|November 1, 1995
Prenatal diagnosis of a (X;X) translocation by fluorescence in situ hybridization and laser scanning image cytometryG Tachdjian, V Cacheux, H Kiefer, et al.
Fetal Diagnosis and Therapy|January 1, 1992
Detection of 47,XYY trophoblast fetal cells in maternal blood by fluorescence in situ hybridization after using immunomagnetic lymphocyte depletion and flow cytometry sortingV Cacheux, C Milesi-Fluet, G Tachdjian, et al.
Human Genetics|January 12, 2001
The human dynein intermediate chain 2 gene (DNAI2): cloning, mapping, expression pattern, and evaluation as a candidate for primary ciliary dyskinesiaG Pennarun, C Chapelin, E Escudier, et al.
Stem Cell Research|April 21, 2019
Generation of induced pluripotent stem cells (iPSCs) IRMBi002-A from an Alzheimer's disease patient carrying a D694N mutation in the APP geneL Auboyer, C Monzo, D Wallon, et al.
Stem Cell Research|January 25, 2019
Generation of induced pluripotent stem cells (IRMBi001-A) from an Alzheimer's disease patient carrying a G217D mutation in the PSEN1 geneL Auboyer, C Monzo, D Wallon, et al.
Human Molecular Genetics|July 13, 2001
Loss-of-function mutations in SIP1 Smad interacting protein 1 result in a syndromic Hirschsprung diseaseV Cacheux, F Dastot-Le Moal, H Kääriäinen, et al.
Cancer Genetics and Cytogenetics|November 11, 1998
Pentasomy 13q in a case of acute myelogenous leukemia (Mo)S Ramond, V Cacheux, M Ciaudo, et al.
Leukemia|September 26, 1997
ETV6 is the target of chromosome 12p deletions in t(12;21) childhood acute lymphocytic leukemiaH Cavé, V Cacheux, S Raynaud, et al.
American Journal of Human Genetics|December 1, 1999
Loss-of-function mutations in a human gene related to Chlamydomonas reinhardtii dynein IC78 result in primary ciliary dyskinesiaG Pennarun, E Escudier, C Chapelin, et al.
Pageof 3

Showing results (11-20 of 28) with videos related to

Sort By:
Pageof 3
American Journal of Medical Genetics|April 6, 1999
De novo inverted duplication 9p21pter involving telomeric repeated sequencesD Sanlaville, C Baumann, J M Lapierre, et al.
Fetal Diagnosis and Therapy|November 1, 1995
Prenatal diagnosis of a (X;X) translocation by fluorescence in situ hybridization and laser scanning image cytometryG Tachdjian, V Cacheux, H Kiefer, et al.
Fetal Diagnosis and Therapy|January 1, 1992
Detection of 47,XYY trophoblast fetal cells in maternal blood by fluorescence in situ hybridization after using immunomagnetic lymphocyte depletion and flow cytometry sortingV Cacheux, C Milesi-Fluet, G Tachdjian, et al.
Human Genetics|January 12, 2001
The human dynein intermediate chain 2 gene (DNAI2): cloning, mapping, expression pattern, and evaluation as a candidate for primary ciliary dyskinesiaG Pennarun, C Chapelin, E Escudier, et al.
Stem Cell Research|April 21, 2019
Generation of induced pluripotent stem cells (iPSCs) IRMBi002-A from an Alzheimer's disease patient carrying a D694N mutation in the APP geneL Auboyer, C Monzo, D Wallon, et al.
Stem Cell Research|January 25, 2019
Generation of induced pluripotent stem cells (IRMBi001-A) from an Alzheimer's disease patient carrying a G217D mutation in the PSEN1 geneL Auboyer, C Monzo, D Wallon, et al.
Human Molecular Genetics|July 13, 2001
Loss-of-function mutations in SIP1 Smad interacting protein 1 result in a syndromic Hirschsprung diseaseV Cacheux, F Dastot-Le Moal, H Kääriäinen, et al.
Cancer Genetics and Cytogenetics|November 11, 1998
Pentasomy 13q in a case of acute myelogenous leukemia (Mo)S Ramond, V Cacheux, M Ciaudo, et al.
Leukemia|September 26, 1997
ETV6 is the target of chromosome 12p deletions in t(12;21) childhood acute lymphocytic leukemiaH Cavé, V Cacheux, S Raynaud, et al.
American Journal of Human Genetics|December 1, 1999
Loss-of-function mutations in a human gene related to Chlamydomonas reinhardtii dynein IC78 result in primary ciliary dyskinesiaG Pennarun, E Escudier, C Chapelin, et al.
Pageof 3