Search Results - Monies, D.M

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  1. 1
    Novel B4GALNT1 mutations in a complicated form of hereditary spastic paraplegia

    Novel B4GALNT1 mutations in a complicated form of hereditary spastic paraplegia by Wakil, S.M., Monies, D.M., Ramzan, K., Hagos, S., Bastaki, L., Meyer, B.F., Bohlega, S.

    Published in Clinical genetics
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  2. 2
    P2.29 Autosomal recessive limb girdle muscular dystrophy in Saudi Arabia

    P2.29 Autosomal recessive limb girdle muscular dystrophy in Saudi Arabia by Al-Muhaizea, M.A, Bohlega, S, Al Homoud, I, Monies, D.M, Majid, S, Al Azami, A, Jaroudi, D, Bas, B, Meyer, B.F, Al Hindi, H.N

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