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searching for TBCE 5 found (10 total)

alternate case: tBCE

Mitochondrial ribosomal protein L32 (627 words) [view diff] case mismatch in snippet view article find links to article

et al. (2003). "Missense mutation in the tubulin-specific chaperone E (Tbce) gene in the mouse mutant progressive motor neuronopathy, a model of human

ARID4B (492 words) [view diff] case mismatch in snippet view article find links to article

Sendtner M (2003). "Missense mutation in the tubulin-specific chaperone E (Tbce) gene in the mouse mutant progressive motor neuronopathy, a model of human

GGPS1 (746 words) [view diff] case mismatch in snippet view article find links to article

(November 2002). "Missense mutation in the tubulin-specific chaperone E (Tbce) gene in the mouse mutant progressive motor neuronopathy, a model of human

Kenny-Caffey syndrome (1,272 words) [view diff] exact match in snippet view article find links to article

Diaz GA, Weiner R, Khan KT, Gordon R, Gelb BD (November 2002). "Mutation of TBCE causes hypoparathyroidism-retardation-dysmorphism and autosomal recessive

PSMA2 (2,990 words) [view diff] case mismatch in snippet view article find links to article

(November 2002). "Missense mutation in the tubulin-specific chaperone E (Tbce) gene in the mouse mutant progressive motor neuronopathy, a model of human