Distal spinal muscular atrophy with vocal cord paralysis (dSMA-VII) is not linked to the MPD2 locus on chromosome 5q31

Por McENTAGART, M., SPURLOCK, G., JACKSON, C., HARPER, P., RAHMAN, N.
Publicado em 2000

Molecular characterisation of a proximal chromosome 18q deletion

Por McENTAGART, M, CAREY, A, BREEN, C, McQUAID, S, STALLINGS, R, GREEN, A, KING, M
Publicado em 2001

Clinical and genetic heterogeneity in peroneal muscular atrophy associated with vocal cord weakness

Por McEntagart, M, Dunstan, M, Bell, C, Boltshauser, E, Donaghy, M, Harper, P, Williams, N, Teare, M, Rahman, N
Publicado em 2002

A new explanation for recessive myotonia congenita: Exon deletions and duplications in CLCN1

Por Raja Rayan, D.L., Haworth, A., Sud, R., Matthews, E., Fialho, D., Burge, J., Portaro, S., Schorge, S., Tuin, K., Lunt, P., McEntagart, M., Toscano, A., Davis, M.B., Hanna, M.G.
Publicado em 2012

TRPV4 mutations and cytotoxic hypercalcemia in axonal Charcot-Marie-Tooth neuropathies

Por Klein, C.J., Shi, Y., Fecto, F., Donaghy, M., Nicholson, G., McEntagart, M.E., Crosby, A.H., Wu, Y., Lou, H., McEvoy, K.M., Siddique, T., Deng, H.-X., Dyck, P.J.
Publicado em 2011