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M Le Lorc'h

Showing results (1-10 of 8) with videos related to

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Human Reproduction (Oxford, England)|October 27, 2001
Assisting reproduction of infertile men carrying a Robertsonian translocationN Frydman, S Romana, M Le Lorc'h, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|February 1, 1993
Per-urethral transvesical first-trimester amniocentesisR Frydman, J C Pons, E Borghi, et al.
American Journal of Medical Genetics. Part A|January 24, 2009
Molecular cytogenetic characterization of a 4p15.1-pter duplication and a 4q35.1-qter deletion in a recombinant of chromosome 4 pericentric inversionM-L Maurin, P Labrune, S Brisset, et al.
American Journal of Medical Genetics. Part A|October 6, 2006
Terminal 14q32.33 deletion: genotype-phenotype correlationM-L Maurin, S Brisset, M Le Lorc'h, et al.
Cytogenetic and Genome Research|May 3, 2013
Molecular and phenotypic characterization of ring chromosome 22 in two unrelated patientsH Hannachi, S Mougou, I Benabdallah, et al.
Annales De Biologie Clinique|March 30, 2004
[A preliminary study to assess the value of the DNA chips SpectralChip to detect subtle constitutional chromosome imbalances]J-M Lapierre, D Sanlaville, J Kang, et al.
American Journal of Medical Genetics. Part A|September 21, 2004
Classical West "syndrome" phenotype with a subtelomeric 4p trisomyMarion Gérard-Blanluet, S Romana, C Munier, et al.
Prenatal Diagnosis|February 4, 2015
Non-invasive prenatal testing for trisomy 21 based on analysis of cell-free fetal DNA circulating in the maternal plasmaA Alberti, L J Salomon, M Le Lorc'h, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Human Reproduction (Oxford, England)|October 27, 2001
Assisting reproduction of infertile men carrying a Robertsonian translocationN Frydman, S Romana, M Le Lorc'h, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|February 1, 1993
Per-urethral transvesical first-trimester amniocentesisR Frydman, J C Pons, E Borghi, et al.
American Journal of Medical Genetics. Part A|January 24, 2009
Molecular cytogenetic characterization of a 4p15.1-pter duplication and a 4q35.1-qter deletion in a recombinant of chromosome 4 pericentric inversionM-L Maurin, P Labrune, S Brisset, et al.
American Journal of Medical Genetics. Part A|October 6, 2006
Terminal 14q32.33 deletion: genotype-phenotype correlationM-L Maurin, S Brisset, M Le Lorc'h, et al.
Cytogenetic and Genome Research|May 3, 2013
Molecular and phenotypic characterization of ring chromosome 22 in two unrelated patientsH Hannachi, S Mougou, I Benabdallah, et al.
Annales De Biologie Clinique|March 30, 2004
[A preliminary study to assess the value of the DNA chips SpectralChip to detect subtle constitutional chromosome imbalances]J-M Lapierre, D Sanlaville, J Kang, et al.
American Journal of Medical Genetics. Part A|September 21, 2004
Classical West "syndrome" phenotype with a subtelomeric 4p trisomyMarion Gérard-Blanluet, S Romana, C Munier, et al.
Prenatal Diagnosis|February 4, 2015
Non-invasive prenatal testing for trisomy 21 based on analysis of cell-free fetal DNA circulating in the maternal plasmaA Alberti, L J Salomon, M Le Lorc'h, et al.
Pageof 1