Sarda P

References (2)

Title : Efficient strategy for the molecular diagnosis of intellectual disability using targeted high-throughput sequencing - Redin_2014_J.Med.Genet_51_724
Author(s) : Redin C , Gerard B , Lauer J , Herenger Y , Muller J , Quartier A , Masurel-Paulet A , Willems M , Lesca G , El-Chehadeh S , Le Gras S , Vicaire S , Philipps M , Dumas M , Geoffroy V , Feger C , Haumesser N , Alembik Y , Barth M , Bonneau D , Colin E , Dollfus H , Doray B , Delrue MA , Drouin-Garraud V , Flori E , Fradin M , Francannet C , Goldenberg A , Lumbroso S , Mathieu-Dramard M , Martin-Coignard D , Lacombe D , Morin G , Polge A , Sukno S , Thauvin-Robinet C , Thevenon J , Doco-Fenzy M , Genevieve D , Sarda P , Edery P , Isidor B , Jost B , Olivier-Faivre L , Mandel JL , Piton A
Ref : Journal of Medical Genetics , 51 :724 , 2014
PubMedID: 25167861
Gene_locus related to this paper: human-NLGN3

Title : [Erythroblastopenia during recurrence of a thymoma associated with myasthenia gravis. Apropos of a new case]. [Spanish] - Montserrat_1996_Sangre_41_249
Author(s) : Montserrat I , Sarda P , Lopez R , Illa I , Bordes R , Ayats R
Ref : Sangre , 41 :249 , 1996
PubMedID: 8755214