The natural history of infantile neuroaxonal dystrophy von Altuame, Fadie D., Foskett, Gretchen, Atwal, Paldeep S., Endemann, Sarah, Midei, Mark, Milner, Peter, Salih, Mustafa A., Hamad, Muddathir, Al-Muhaizea, Mohammad, Hashem, Mais, Alkuraya, Fowzan S.

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PLXNA2 as a candidate gene in patients with intellectual disability von Altuame, Fadie D., Shamseldin, Hanan E., Albatti, Turki H., Hashem, Mais, Ewida, Nour, Abdulwahab, Firdous, Alkuraya, Fowzan S.

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Further delineation of MYO18B‐related autosomal recessive Klippel‐Feil syndrome with myopathy and facial dysmorphism von Altuame, Fadie D., Haldeman‐Englert, Chad, Cupler, Edward, Al Muhaizea, Mohammad A., Al‐Zaidan, Hamad I., Hashem, Mais, Alkuraya, Fowzan S.

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Additional file 2 of The natural history of infantile neuroaxonal dystrophy von Fadie D. Altuame, Foskett, Gretchen, Paldeep S. Atwal, Endemann, Sarah, Midei, Mark, Milner, Peter, Salih, Mustafa A., Muddathir Hamad, Al-Muhaizea, Mohammad, Hashem, Mais, Fowzan S. Alkuraya

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PLXNA2 as a candidate gene in patients with intellectual disability von Altuame, Fadie D, Shamseldin, Hanan E, Albatti, Turki H, Hashem, Mais, Ewida, Nour, Abdulwahab, Firdous, Alkuraya, Fowzan S

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Additional file 1 of The natural history of infantile neuroaxonal dystrophy von Fadie D. Altuame, Foskett, Gretchen, Paldeep S. Atwal, Endemann, Sarah, Midei, Mark, Milner, Peter, Salih, Mustafa A., Muddathir Hamad, Al-Muhaizea, Mohammad, Hashem, Mais, Fowzan S. Alkuraya

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