Biblio

33 resultats trouvés
Filtres: Auteur is Sanlaville, D.  [Clear All Filters]
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Delanne J., Nambot S., Chassagne A., Putois O., Pelissier A., Peyron C., Gautier E., Thevenon J., Cretin E., Bruel A.L et al..  2019.  Secondary findings from whole-exome/genome sequencing evaluating stakeholder perspectives. A review of the literature. EUROPEAN JOURNAL OF MEDICAL GENETICS. 62:103529.
Chassagne A., Pelissier A., Peyron C., Houdayer F., Salvi D., Kidri S., Charpin A., Godard A., Putois O., Thauvin-Robinet C. et al..  2018.  SEQUAPRE: Preferences and representations from patients and parents with regard to the use of Next-Generation Sequencing technologies in medical genetics. The case of development anomalies. EUROPEAN JOURNAL OF HUMAN GENETICS. 26:69-70.
Chassagne A., Pelissier A., Peyron C., Houdayer F., Salvi D., Kidri S., Charpin A., Godard A., Putois O., Thauvin-Robinet C. et al..  2018.  SEQUAPRE: Preferences and representations from patients and parents with regard to the use of Next-Generation Sequencing technologies in medical genetics. The case of development anomalies. EUROPEAN JOURNAL OF HUMAN GENETICS. 26:69-70.
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Chatron N., Giannuzzi G., Rollat-Farnier P., Diguet F., Porcu E., Yammine T., Uguen K., Bellil Z., J. Zillhardt L, Sorlin A. et al..  2020.  The enrichment of breakpoints in late-replicating chromatin provides novel insights into chromoanagenesis mechanisms. EUROPEAN JOURNAL OF HUMAN GENETICS. 28:5-6.
Houdayer F., Chassagne A., Pelissier A., Peyron C., Staraci S., Sanlaville D., Edery P., Rossi M., Lesca G., Putoux A. et al..  2019.  The French FIND study (preliminary results). Psychological effects of actionable secondary findings obtained from exome sequencing in patients/families with undiagnosed rare diseases. EUROPEAN JOURNAL OF HUMAN GENETICS. 27:1151-1152.
Houdayer F., Chassagne A., Pelissier A., Peyron C., Staraci S., Sanlaville D., Edery P., Rossi M., Lesca G., Putoux A. et al..  2019.  The French FIND study (preliminary results). Psychological effects of actionable secondary findings obtained from exome sequencing in patients/families with undiagnosed rare diseases. EUROPEAN JOURNAL OF HUMAN GENETICS. 27:1151-1152.
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Schluth-Bolard C., Diguet F., Rollat-Farnier P.A, Amiel J., Belaud-Rotureau M.A, Benzacken B., Callier P., Chatron N., Collignon P., Demeer B. et al..  2018.  Unravelling structural chromosomal rearrangements by whole genome sequencing: results of the ANI project, a French collaborative study including 55 patients with intellectual disability and/or congenital malformations. EUROPEAN JOURNAL OF HUMAN GENETICS. 26:628-629.
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Chatron N., Diguet F., Rollat-Farnier P., Uguen K., J. Zillhardt L, Sorlin A., Andrieux J., Chantot-Bastaraud S., Callier P., Cordier M. et al..  2019.  Whole Genome Sequencing of 9 patients allowed a better understanding of complex chromosomal rearrangements. EUROPEAN JOURNAL OF HUMAN GENETICS. 27:479-480.

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