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thalassemic Meaning in marathi ( thalassemic शब्दाचा मराठी अर्थ)



थॅलेसेमिक

Noun:

थॅलेसेमिया,



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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