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C Turleau

Showing results (141-150 of 155) with videos related to

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Human Reproduction (Oxford, England)|January 5, 2001
Chromosomal factors of infertility in candidate couples for ICSI: an equal risk of constitutional aberrations in women and menJ Gekas, F Thepot, C Turleau, et al.
Clinical Genetics|November 29, 2007
Sotos syndrome caused by a paracentric inversion disrupting the NSD1 geneV Malan, M C De Blois, M Prieur, et al.
Journal of Medical Genetics|January 8, 2009
19q13.11 deletion syndrome: a novel clinically recognisable genetic condition identified by array comparative genomic hybridisationV Malan, O Raoul, H V Firth, et al.
Annales De Genetique|January 1, 1985
Embryonic testicular regression syndrome and severe mental retardation in sibsJ de Grouchy, A Gompel, Y Salomon-Bernard, et al.
Clinical Genetics|October 12, 2001
Comparative genomic hybridisation in mentally retarded patients with dysmorphic features and a normal karyotypeG Joly, J M Lapierre, C Ozilou, et al.
Clinical Genetics|October 16, 2012
Monozygotic twins discordant for submicroscopic chromosomal anomalies in 2p25.3 region detected by array CGHM Rio, G Royer, S Gobin, et al.
Journal of Medical Genetics|August 6, 2002
Deletion of the SIM1 gene (6q16.2) in a patient with a Prader-Willi-like phenotypeL Faivre, V Cormier-Daire, J M Lapierre, et al.
Clinical Genetics|February 14, 2015
Xq25 duplication: the crucial role of the STAG2 gene in this novel human cohesinopathyC Leroy, M-L Jacquemont, B Doray, et al.
Clinical Genetics|April 10, 2002
A CGH study of 27 patients with CHARGE associationD Sanlaville, S P Romana, J M Lapierre, 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.
Pageof 16

Showing results (141-150 of 155) with videos related to

Sort By:
Pageof 16
Human Reproduction (Oxford, England)|January 5, 2001
Chromosomal factors of infertility in candidate couples for ICSI: an equal risk of constitutional aberrations in women and menJ Gekas, F Thepot, C Turleau, et al.
Clinical Genetics|November 29, 2007
Sotos syndrome caused by a paracentric inversion disrupting the NSD1 geneV Malan, M C De Blois, M Prieur, et al.
Journal of Medical Genetics|January 8, 2009
19q13.11 deletion syndrome: a novel clinically recognisable genetic condition identified by array comparative genomic hybridisationV Malan, O Raoul, H V Firth, et al.
Annales De Genetique|January 1, 1985
Embryonic testicular regression syndrome and severe mental retardation in sibsJ de Grouchy, A Gompel, Y Salomon-Bernard, et al.
Clinical Genetics|October 12, 2001
Comparative genomic hybridisation in mentally retarded patients with dysmorphic features and a normal karyotypeG Joly, J M Lapierre, C Ozilou, et al.
Clinical Genetics|October 16, 2012
Monozygotic twins discordant for submicroscopic chromosomal anomalies in 2p25.3 region detected by array CGHM Rio, G Royer, S Gobin, et al.
Journal of Medical Genetics|August 6, 2002
Deletion of the SIM1 gene (6q16.2) in a patient with a Prader-Willi-like phenotypeL Faivre, V Cormier-Daire, J M Lapierre, et al.
Clinical Genetics|February 14, 2015
Xq25 duplication: the crucial role of the STAG2 gene in this novel human cohesinopathyC Leroy, M-L Jacquemont, B Doray, et al.
Clinical Genetics|April 10, 2002
A CGH study of 27 patients with CHARGE associationD Sanlaville, S P Romana, J M Lapierre, 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.
Pageof 16