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Annals of Hematology|December 4, 2008
The Hellenic type of nondeletional hereditary persistence of fetal hemoglobin results from a novel mutation (g.-109G>T) in the HBG2 gene promoterChristos Chassanidis, Angelos Kalamaras, Marios Phylactides, et al.
Cell Structure and Function|February 1, 1997
Assemblases and coupling proteins in thick filament assemblyF Liu, J M Barral, C C Bauer, et al.
The Journal of Comparative Neurology|May 14, 1998
Developmental changes in expression of myotonic dystrophy protein kinase in the rat central nervous systemA Balasubramanyam, D Iyer, J L Stringer, et al.
Neurosurgery|January 11, 2001
Natural history of brainstem cavernous malformationsM J Kupersmith, H Kalish, F Epstein, et al.
Neurology|December 15, 2004
Diffusion tensor imaging for the assessment of upper motor neuron integrity in ALSJ M Graham, N Papadakis, J Evans, et al.
Pediatrics|September 1, 1988
Bilirubin, intraventricular hemorrhage, and phenobarbital in very low birth weight babiesM F Epstein, A Leviton, K C Kuban, et al.
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