APA
Nambot S., Thevenon J., Kuentz P., Duffourd Y., Tisserant E., Bruel A., Mosca-Boidron A., Masurel-Paulet A., Lehalle D., Jean-Marçais N., Lefebvre M., Vabres P., El Chehadeh-Djebbar S., Philippe C., Tran Mau-Them F., St-Onge J., Jouan T., Chevarin M., Poé C., Carmignac V., Vitobello A., Callier P., Rivière J., Faivre L. & Thauvin-Robinet C. (20181017). Clinical whole-exome sequencing for the diagnosis of rare disorders with congenital anomalies and/or intellectual disability: substantial interest of prospective annual reanalysis. : Genetics in medicine : official journal of the American College of Medical Genetics.
Chicago
Nambot Sophie, Thevenon Julien, Kuentz Paul, Duffourd Yannis, Tisserant Emilie, Bruel Ange-Line, Mosca-Boidron Anne-Laure, Masurel-Paulet Alice, Lehalle Daphné, Jean-Marçais Nolwenn, Lefebvre Mathilde, Vabres Pierre, El Chehadeh-Djebbar Salima, Philippe Christophe, Tran Mau-Them Frederic, St-Onge Judith, Jouan Thibaud, Chevarin Martin, Poé Charlotte, Carmignac Virginie, Vitobello Antonio, Callier Patrick, Rivière Jean-Baptiste, Faivre Laurence and Thauvin-Robinet Christel. 20181017. Clinical whole-exome sequencing for the diagnosis of rare disorders with congenital anomalies and/or intellectual disability: substantial interest of prospective annual reanalysis. : Genetics in medicine : official journal of the American College of Medical Genetics.
Harvard
Nambot S., Thevenon J., Kuentz P., Duffourd Y., Tisserant E., Bruel A., Mosca-Boidron A., Masurel-Paulet A., Lehalle D., Jean-Marçais N., Lefebvre M., Vabres P., El Chehadeh-Djebbar S., Philippe C., Tran Mau-Them F., St-Onge J., Jouan T., Chevarin M., Poé C., Carmignac V., Vitobello A., Callier P., Rivière J., Faivre L. and Thauvin-Robinet C. (20181017). Clinical whole-exome sequencing for the diagnosis of rare disorders with congenital anomalies and/or intellectual disability: substantial interest of prospective annual reanalysis. : Genetics in medicine : official journal of the American College of Medical Genetics.
MLA
Nambot Sophie, Thevenon Julien, Kuentz Paul, Duffourd Yannis, Tisserant Emilie, Bruel Ange-Line, Mosca-Boidron Anne-Laure, Masurel-Paulet Alice, Lehalle Daphné, Jean-Marçais Nolwenn, Lefebvre Mathilde, Vabres Pierre, El Chehadeh-Djebbar Salima, Philippe Christophe, Tran Mau-Them Frederic, St-Onge Judith, Jouan Thibaud, Chevarin Martin, Poé Charlotte, Carmignac Virginie, Vitobello Antonio, Callier Patrick, Rivière Jean-Baptiste, Faivre Laurence and Thauvin-Robinet Christel. Clinical whole-exome sequencing for the diagnosis of rare disorders with congenital anomalies and/or intellectual disability: substantial interest of prospective annual reanalysis. : Genetics in medicine : official journal of the American College of Medical Genetics. 20181017.