<p>Letters C, E and P next to the 8+1 MT pattern denote position of a transposed doublet in the axoneme: central, eccentric and at the perimeter, respectively. Nd: cross-section plane and the presence of microvilli not determined, due to the low number of ciliary cross-sections.</p
Primary ciliary dyskinesia (PCD) is a genetically heterogeneous inherited disorder arising from dysm...
Primary ciliary dyskinesia (PCD) is a rare autosomal-recessive respiratory disorder resulting from d...
Primary ciliary dyskinesia (PCD) is a rare, autosomal recessive, genetically heterogeneous disorder ...
<p><b>A</b> Ciliary cross sections – magnification 30,000 (patient #181). <i>Left panel</i> – a typi...
Primary ciliary dyskinesia (PCD) is a genetically heterogeneous recessive disorder caused by several...
Primary ciliary dyskinesia (PCD) is a genetically heterogeneous recessive disorder caused by several...
Primary ciliary dyskinesia (PCD) is a rare (1/20,000), multisystem disease with a complex phenotype ...
Primary ciliary dyskinesia (PCD) is a rare (1/20,000), multisystem disease with a complex phenotype ...
Diagnosis testing for primary ciliary dyskinesia (PCD) requires a combination of investigations that...
Primary ciliary dyskinesia (PCD) is an inherited chronic respiratory obstructive disease with random...
International audiencePrimary ciliary dyskinesia (PCD) is a rare autosomal-recessive condition resul...
<p>(A–G) Immunofluorescent staining of hTERT-RPE1 cells transfected with empty vector (EV), sh<i>BBS...
International audiencePrimary ciliary dyskinesia (PCD) is a rare autosomal-recessive respiratory dis...
Primary ciliary dyskinesia (PCD) is a rare autosomal-recessive condition resulting from structural a...
The radial spoke head protein 4 homolog A (RSPH4A) gene is one of more than 50 genes that cause Prim...
Primary ciliary dyskinesia (PCD) is a genetically heterogeneous inherited disorder arising from dysm...
Primary ciliary dyskinesia (PCD) is a rare autosomal-recessive respiratory disorder resulting from d...
Primary ciliary dyskinesia (PCD) is a rare, autosomal recessive, genetically heterogeneous disorder ...
<p><b>A</b> Ciliary cross sections – magnification 30,000 (patient #181). <i>Left panel</i> – a typi...
Primary ciliary dyskinesia (PCD) is a genetically heterogeneous recessive disorder caused by several...
Primary ciliary dyskinesia (PCD) is a genetically heterogeneous recessive disorder caused by several...
Primary ciliary dyskinesia (PCD) is a rare (1/20,000), multisystem disease with a complex phenotype ...
Primary ciliary dyskinesia (PCD) is a rare (1/20,000), multisystem disease with a complex phenotype ...
Diagnosis testing for primary ciliary dyskinesia (PCD) requires a combination of investigations that...
Primary ciliary dyskinesia (PCD) is an inherited chronic respiratory obstructive disease with random...
International audiencePrimary ciliary dyskinesia (PCD) is a rare autosomal-recessive condition resul...
<p>(A–G) Immunofluorescent staining of hTERT-RPE1 cells transfected with empty vector (EV), sh<i>BBS...
International audiencePrimary ciliary dyskinesia (PCD) is a rare autosomal-recessive respiratory dis...
Primary ciliary dyskinesia (PCD) is a rare autosomal-recessive condition resulting from structural a...
The radial spoke head protein 4 homolog A (RSPH4A) gene is one of more than 50 genes that cause Prim...
Primary ciliary dyskinesia (PCD) is a genetically heterogeneous inherited disorder arising from dysm...
Primary ciliary dyskinesia (PCD) is a rare autosomal-recessive respiratory disorder resulting from d...
Primary ciliary dyskinesia (PCD) is a rare, autosomal recessive, genetically heterogeneous disorder ...