thalassemic Meaning in Telugu ( thalassemic తెలుగు అంటే)
తలసెమిక్, తలన్రేలు చేయు
Noun:
తలన్రేలు చేయు,
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thalassemic's Usage Examples:
snRNAs promote efficient skipping of an aberrant exon in three human beta-thalassemic mutations".
disease require a pre-existing medical condition, usually associated with thalassemic hemoglobinopathy.
(GGT-->CGT)] is a typical alpha chain hemoglobinopathy without an alpha-thalassemic effect".
Physical growth parameters in thalassemic children.
present as beta thalassemia silent carriers; those who inherit a beta thalassemic mutation but have no hematologic abnormalities nor symptoms.
decree (1996) Prevention of thalassemic child birth ( c.
"Discrimination indices as screening tests for beta-thalassemic trait".
: Translation of rabbit haemoglobin messenger RNA by thalassemic and non-thalassemic ribosomes.
The serial analyses of β-thalassemic mice indicate hemoglobin levels decreases over time, while the concentration.
"Base substitution at position -88 in a beta-thalassemic globin gene.
"Restoration of correct splicing in thalassemic pre-mRNA by antisense oligonucleotides".
molecular characterization of the --CAMPANIA deletion, a novel alpha (0) -thalassemic defect, in two unrelated Italian families [corrected]".
"Expression of microRNA-451 in normal and thalassemic erythropoiesis".
CGT)] is a typical alpha chain hemoglobinopathy without an alpha-thalassemic effect".
Physical growth parameters in thalassemic children.
present as beta thalassemia silent carriers; those who inherit a beta thalassemic mutation but have no hematologic abnormalities nor symptoms.
decree (1996) Prevention of thalassemic child birth ( c.
"Discrimination indices as screening tests for beta-thalassemic trait".
: Translation of rabbit haemoglobin messenger RNA by thalassemic and non-thalassemic ribosomes.
The serial analyses of β-thalassemic mice indicate hemoglobin levels decreases over time, while the concentration.
"Base substitution at position -88 in a beta-thalassemic globin gene.
"Restoration of correct splicing in thalassemic pre-mRNA by antisense oligonucleotides".
molecular characterization of the --CAMPANIA deletion, a novel alpha (0) -thalassemic defect, in two unrelated Italian families [corrected]".
"Expression of microRNA-451 in normal and thalassemic erythropoiesis".
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