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European Journal of Pharmacology|January 14, 1997
Extracellular aspartate concentration increases in nucleus accumbens after cocaine sensitizationS E Robinson, P M Kunko, J A Smith, et al.
Proteomics|January 4, 2005
Housekeeping proteins: a preliminary study illustrating some limitations as useful references in protein expression studiesRoisean E Ferguson, Helen P Carroll, Adrian Harris, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|January 19, 2013
Mild and severe congenital primary hypothyroidism in two patients by thyrotropin receptor (TSHR) gene mutationVeysel Nijat Baş, Hakan Cangul, Sebahat Yilmaz Agladioglu, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|October 16, 2013
A truncating DUOX2 mutation (R434X) causes severe congenital hypothyroidismHakan Cangul, Zehra Aycan, Michaela Kendall, et al.
The Journal of Speech and Hearing Disorders|May 1, 1990
Communication disorders and emotional/behavioral disorders in children and adolescentsB M Prizant, L R Audet, G M Burke, et al.
Journal of Medical Genetics|February 12, 2002
A locus for isolated cataract on human XpP J Francis, V Berry, A J Hardcastle, et al.
Journal of the National Cancer Institute|August 30, 2008
Germline SDHB mutations and familial renal cell carcinomaChristopher Ricketts, Emma R Woodward, Pip Killick, et al.
Optics Letters|November 1, 2014
In vivo analysis of burns in a mouse model using spectroscopic optical coherence tomographyJason R Maher, Volker Jaedicke, Manuel Medina, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|October 26, 2013
A common thyroid peroxidase gene mutation (G319R) in Turkish patients with congenital hypothyroidism could be due to a founder effectVeysel Nijat Baş, Zehra Aycan, Hakan Cangul, et al.
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