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Intragenic FMR1 disease-causing variants: a significant mut..:
Quartier, Angélique
;
Poquet, Hélène
;
Gilbert-Dussardier, Brigitte
...
European Journal of Human Genetics. 25 (2017) 4 - p. 423-431 , 2017
Link:
https://doi.org/10.1038/ejhg.2016.204
RT Journal T1
Intragenic FMR1 disease-causing variants: a significant mutational mechanism leading to Fragile-X syndrome
UL https://suche.suub.uni-bremen.de/peid=cr-10.1038_ejhg.2016.204&Exemplar=1&LAN=DE A1 Quartier, Angélique A1 Poquet, Hélène A1 Gilbert-Dussardier, Brigitte A1 Rossi, Massimiliano A1 Casteleyn, Anne-Sophie A1 Portes, Vincent des A1 Feger, Claire A1 Nourisson, Elsa A1 Kuentz, Paul A1 Redin, Claire A1 Thevenon, Julien A1 Mosca-Boidron, Anne-Laure A1 Callier, Patrick A1 Muller, Jean A1 Lesca, Gaetan A1 Huet, Frédéric A1 Geoffroy, Véronique A1 El Chehadeh, Salima A1 Jung, Matthieu A1 Trojak, Benoit A1 Le Gras, Stéphanie A1 Lehalle, Daphné A1 Jost, Bernard A1 Maury, Stéphanie A1 Masurel, Alice A1 Edery, Patrick A1 Thauvin-Robinet, Christel A1 Gérard, Bénédicte A1 Mandel, Jean-Louis A1 Faivre, Laurence PB Springer Science and Business Media LLC YR 2017 SN 1018-4813 SN 1476-5438 JF European Journal of Human Genetics VO 25 IS 4 SP 423 OP 431 LK http://dx.doi.org/https://doi.org/10.1038/ejhg.2016.204 DO https://doi.org/10.1038/ejhg.2016.204 SF ELIB - SuUB Bremen
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