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Cytogenetic and Genome Research|September 24, 2015
Small Supernumerary Marker Chromosomes in Human InfertilityNarjes Armanet, Lucie Tosca, Sophie Brisset, et al.
Fetal Diagnosis and Therapy|August 17, 2006
Early and rapid prenatal diagnosis of monosomy 2q36.1 in trophoblast cellsGérard Tachdjian, Azzedine Aboura, Sophie Brisset, et al.
Annales De Biologie Clinique|August 1, 2025
[Example of a genetic condition caused by an imprinting disorder: Angelman syndrome]Charlene Coquisart, Sana Skouri, Geoffroy Delplancq, et al.
Frontiers in Cardiovascular Medicine|September 30, 2021
Case Report: <i>BMPR2</i>-Targeted MinION Sequencing as a Tool for Genetic Analysis in Patients With Pulmonary Arterial HypertensionTomoya Takashima, Sophie Brisset, Asuka Furukawa, et al.
Case Reports in Pediatrics|November 28, 2025
Severe Neurodevelopmental Disorder due to Klinefelter Syndrome and <i>CACNA1C</i> Variant: A Case ReportImen El Kamel El Lebbi, Séverine Bacrot, Myrtille Spentchian, et al.
BMC Health Services Research|December 25, 2019
Lack of consensus in the choice of termination of pregnancy for Turner syndrome in FranceMonika Hermann, Babak Khoshnood, Olivia Anselem, et al.
Reproductive Biomedicine Online|December 7, 2018
Chromosomal translocations and semen quality: A study on 144 male translocation carriersAnne Mayeur, Naouel Ahdad, Laetitia Hesters, et al.
European Journal of Medical Genetics|September 29, 2012
Small supernumerary marker chromosomes derived from chromosomes 6 and 20 in a woman with recurrent spontaneous abortionsNarjes Guediche, Lucie Tosca, Marc Nouchy, et al.
Journal of Ultrasound in Medicine : Official Journal of the American Institute of Ultrasound in Medicine|November 6, 2023
Prenatal Diagnosis of Primrose SyndromeWael Abdallah, Emmanuel Spaggiari, Sophie Brisset, et al.
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