Detailed mapping, mutation analysis, and intragenic polymorphism identification in candidate Noonan syndrome genes MYL2, DCN, EPS8, and RPL6

Ion, A ; Crosby, A H ; Kremer, H ; Kenmochi, N ; Van Reen, M ; Fenske, C ; Van Der Burgt, I ; Brunner, H G ; Montgomery, K ; Kucherlapati, R S ; Patton, M A ; Page, C ; Mariman, E ; Jeffery, S

Journal of medical genetics, 2000-11, Vol.37 (11), p.884-886 [Periódico revisado por pares]

England: BMJ Group

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