laminopathy

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Congenital Pelger–Huët anomaly. Royalty Free Stock Photo
Lonafarnib drug molecule. Inhibitor of farnesyltransferase. Skeletal formula Royalty Free Stock Photo
Lonafarnib drug molecule. Inhibitor of farnesyltransferase. Skeletal formula Royalty Free Stock Photo
Lonafarnib drug molecule. Inhibitor of farnesyltransferase. 3D rendering. Royalty Free Stock Photo
Lonafarnib drug molecule. Inhibitor of farnesyltransferase. 3D rendering. Royalty Free Stock Photo
Lonafarnib drug molecule. Inhibitor of farnesyltransferase. 3D rendering. Atoms are represented as spheres with conventional color Royalty Free Stock Photo
Lonafarnib drug molecule. Inhibitor of farnesyltransferase. 3D rendering. Atoms are represented as spheres with conventional color Royalty Free Stock Photo
Congenital Pelger–Huët anomaly.
Lonafarnib drug molecule. Inhibitor of farnesyltransferase. 3D rendering. Royalty Free Stock Photo
lonafarnib molecule, farnesyltransferase inhibitor, molecular structure, isolated 3d model van der Waals Royalty Free Stock Photo
lonafarnib molecule, molecular structures, farnesyltransferase inhibitor, 3d model, Structural Chemical Formula and Atoms with Royalty Free Stock Photo
lonafarnib molecule 3d, molecular structure, ball and stick model, structural chemical formula farnesyltransferase inhibitor Royalty Free Stock Photo
lonafarnib molecular structure, 3d model molecule, farnesyltransferase inhibitor, structural chemical formula view from a Royalty Free Stock Photo
lonafarnib molecule, structural chemical formula, ball-and-stick model, isolated image farnesyltransferase inhibitor Royalty Free Stock Photo
lonafarnib molecular structure, 3d model molecule, zokinvy, structural chemical formula view from a microscope Royalty Free Stock Photo
Congenital Pelger–Huët anomaly. It is a blood laminopathy associated with the lamin B receptor, wherein several types of white blood cells (neutrophils and eosinophils) have nuclei with unusual shape. Wright x1000.


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