Typical clinical diagnosis and negative first-line molecular results: when genome sequencing and transcriptomics integration helps untangle unexplained rare Mendelian diseases by Colin, E, Duffourd, Y, Callier, P, Tisserant, E, Besnard, T, Goldenberg, A, Cogne, B, Isidor, B, Sorlin, A, Moutton, S, Delanne, J, Bruel, Al, Mau-Them, Ft, Denomme-Pichon, As, Fradin, M, Dubourg, C, Gorce, M, El Chehadeh, S, Debray, Fg, Fenzy, Md, Uguen, K, Boland, Anne, Olaso, Robert, Deleuze, Jean-François, Sanlaville, D, Philippe, C, Thauvin-Robinet, C, Faivre, L, Vitobello, A

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