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V Malan

Showing results (11-20 of 25) with videos related to

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Human Reproduction (Oxford, England)|April 6, 2006
Chromosome segregation in an infertile man carrying a unique pericentric inversion, inv(21)(p12q22.3), analysed using fluorescence in situ hybridization on sperm nuclei: significance for clinical genetics. A case reportV Malan, E Pipiras, C Sifer, 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.
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.
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.
AJNR. American Journal of Neuroradiology|December 24, 2021
Feasibility and Added Value of Fetal DTI Tractography in the Evaluation of an Isolated Short Corpus Callosum: Preliminary ResultsA-E Millischer, D Grevent, P Sonigo, 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.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|March 27, 2021
Electro-clinical features in epileptic children with chromosome 15q duplication syndromeM-T Dangles, V Malan, G Dumas, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|July 25, 2015
Fetal growth restriction and intra-uterine growth restriction: guidelines for clinical practice from the French College of Gynaecologists and ObstetriciansC Vayssière, L Sentilhes, A Ego, et al.
Pageof 3

Showing results (11-20 of 25) with videos related to

Sort By:
Pageof 3
Human Reproduction (Oxford, England)|April 6, 2006
Chromosome segregation in an infertile man carrying a unique pericentric inversion, inv(21)(p12q22.3), analysed using fluorescence in situ hybridization on sperm nuclei: significance for clinical genetics. A case reportV Malan, E Pipiras, C Sifer, 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.
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.
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.
AJNR. American Journal of Neuroradiology|December 24, 2021
Feasibility and Added Value of Fetal DTI Tractography in the Evaluation of an Isolated Short Corpus Callosum: Preliminary ResultsA-E Millischer, D Grevent, P Sonigo, 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.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|March 27, 2021
Electro-clinical features in epileptic children with chromosome 15q duplication syndromeM-T Dangles, V Malan, G Dumas, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|July 25, 2015
Fetal growth restriction and intra-uterine growth restriction: guidelines for clinical practice from the French College of Gynaecologists and ObstetriciansC Vayssière, L Sentilhes, A Ego, et al.
Pageof 3