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Human Reproduction (Oxford, England)
|
October 27, 2001
Assisting reproduction of infertile men carrying a Robertsonian translocation
N 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 amniocentesis
R 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 inversion
M-L Maurin, P Labrune, S Brisset, et al.
American Journal of Medical Genetics. Part A
|
October 6, 2006
Terminal 14q32.33 deletion: genotype-phenotype correlation
M-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 patients
H 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 trisomy
Marion 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 plasma
A Alberti, L J Salomon, M Le Lorc'h, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 8) with videos related to
Sort By:
Page
of 1
Human Reproduction (Oxford, England)
|
October 27, 2001
Assisting reproduction of infertile men carrying a Robertsonian translocation
N 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 amniocentesis
R 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 inversion
M-L Maurin, P Labrune, S Brisset, et al.
American Journal of Medical Genetics. Part A
|
October 6, 2006
Terminal 14q32.33 deletion: genotype-phenotype correlation
M-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 patients
H 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 trisomy
Marion 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 plasma
A Alberti, L J Salomon, M Le Lorc'h, et al.
Page
of 1