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R Mullaart

Showing results (1-10 of 6) with videos related to

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Journal of Neurology, Neurosurgery, and Psychiatry|May 13, 2006
Arnold-Chiari-II malformation and cognitive functioning in spina bifidaA Vinck, B Maassen, R Mullaart, et al.
European Journal of Ultrasound : Official Journal of the European Federation of Societies for Ultrasound in Medicine and Biology|March 16, 2000
Ultrasonographic assessment of congestion of the choroid plexus in relation to carbon dioxide pressureP Beulen, J Rotteveel, A de Haan, et al.
Brain & Development|January 1, 1982
Familial lissencephaly with extreme neopallial hypoplasiaP G Barth, R Mullaart, F C Stam, et al.
Acta Neuropathologica|January 1, 1983
The neuropathy of Cockayne syndromeA Vos, A Gabreëls-Festen, E Joosten, et al.
Ultrasonic Imaging|May 24, 2000
Calibrated parametric medical ultrasound imagingF M Valckx, J M Thijsse, A J van Geemen, et al.
American Journal of Human Genetics|December 5, 1998
The first nuclear-encoded complex I mutation in a patient with Leigh syndromeJ Loeffen, J Smeitink, R Triepels, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Journal of Neurology, Neurosurgery, and Psychiatry|May 13, 2006
Arnold-Chiari-II malformation and cognitive functioning in spina bifidaA Vinck, B Maassen, R Mullaart, et al.
European Journal of Ultrasound : Official Journal of the European Federation of Societies for Ultrasound in Medicine and Biology|March 16, 2000
Ultrasonographic assessment of congestion of the choroid plexus in relation to carbon dioxide pressureP Beulen, J Rotteveel, A de Haan, et al.
Brain & Development|January 1, 1982
Familial lissencephaly with extreme neopallial hypoplasiaP G Barth, R Mullaart, F C Stam, et al.
Acta Neuropathologica|January 1, 1983
The neuropathy of Cockayne syndromeA Vos, A Gabreëls-Festen, E Joosten, et al.
Ultrasonic Imaging|May 24, 2000
Calibrated parametric medical ultrasound imagingF M Valckx, J M Thijsse, A J van Geemen, et al.
American Journal of Human Genetics|December 5, 1998
The first nuclear-encoded complex I mutation in a patient with Leigh syndromeJ Loeffen, J Smeitink, R Triepels, et al.
Pageof 1