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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.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.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.Prenatal Diagnosis|June 22, 2000
Subtle familial unbalanced translocation t(8;11)(p23.2;p15.5) in two fetuses with Beckwith-Wiedemann featuresS Fert-Ferrer, A Guichet, J Tantau, et al.European Journal of Medical Genetics|July 9, 2013
Monozygotic twins discordant for 18q21.2qter deletion detected by array CGH in amniotic fluidM Essaoui, M Nizon, M P Beaujard, et al.Journal of Medical Genetics|April 16, 2002
Automated fluorescent genotyping detects 10% of cryptic subtelomeric rearrangements in idiopathic syndromic mental retardationM Rio, F Molinari, S Heuertz, et al.European Journal of Human Genetics : EJHG|May 30, 2001
A novel automated strategy for screening cryptic telomeric rearrangements in children with idiopathic mental retardationL Colleaux, M Rio, S Heuertz, et al.Pageof 17