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Pazour, Gregory

One or more keywords matched the following items that are connected to Pazour, Gregory

Item Type	Name
Academic Article	Disruption of Mks1 localization to the mother centriole causes cilia defects and developmental malformations in Meckel-Gruber syndrome.
Concept	Abnormalities, Multiple
Academic Article	Novel Jbts17 mutant mouse model of Joubert syndrome with cilia transition zone defects and cerebellar and other ciliopathy related anomalies.
Academic Article	Fifteen years of research on oral-facial-digital syndromes: from 1 to 16 causal genes.
Academic Article	Super-resolution microscopy reveals that disruption of ciliary transition-zone architecture causes Joubert?syndrome.

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