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Results: 1-4 |
Results: 4

Authors: Hampshire, DJ Roberts, E Crow, Y Bond, J Mubaidin, A Wriekat, AL Al-Din, A Woods, CG
Citation: Dj. Hampshire et al., Kufor-Rakeb syndrome, pallido-pyramidal degeneration with supranuclear upgaze paresis and dementia, maps to 1p36, J MED GENET, 38(10), 2001, pp. 680-682

Authors: Christodoulou, K Zamba, E Tsingis, M Mubaidin, A Horani, K Abu-Sheik, S El-Khateeb, M Kyriacou, K Kyriakides, T Al-Qudah, AK Middleton, L
Citation: K. Christodoulou et al., A novel form of distal hereditary motor neuronopathy maps to chromosome 9p21.1-p12, ANN NEUROL, 48(6), 2000, pp. 877-884

Authors: Middleton, L Ohno, K Christodoulou, K Brengman, J Milone, M Neocleous, V Serdaroglu, P Deymeer, F Ozdemir, C Mubaidin, A Horany, K Al-Shehab, A Mavromatis, I Mylonas, I Tsingis, M Zamba, E Pantzaris, M Kyriallis, K Engel, AG
Citation: L. Middleton et al., Chromosome 17p-linked myasthenias stem from defects in the acetylcholine receptor epsilon-subunit gene, NEUROLOGY, 53(5), 1999, pp. 1076-1082

Authors: Fang, Y Lepont, P Fassett, JT Ford, SP Mubaidin, A Hamilton, RT Nilsen-Hamilton, M
Citation: Y. Fang et al., Signaling between the placenta and the uterus involving the mitogen-regulated protein/proliferins, ENDOCRINOL, 140(11), 1999, pp. 5239-5249
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