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Cerebellar malformations Total agenesis rare, often associated with hypoplasticdysplastic pontine nuclei and inferior olives; may see with large occipital encephaloceles Aplasia of vermis Seen in Dandy-Walker syndrome Joubert syndrome Episodic hyperpnea, abnormal eye move- ments, ataxia, and mental retardation High incidence of death in infantile period Cerebral hemispheres largely unaffected 4th ventricle dilated Rhombencephalosynopsis-fusion of the cere- bellar hemispheres and dentate across the midline Pontoneocerebellar hypoplasia Microcephaly Hypoplastic cerebellar hemispheres Dentate nuclei disorganized Death by age 2 years Granular cell aplasia Cerebellar heterotopia-ectopic gray matter in cerebellar white matter, more common in hemi- spheres Cerebellar dysplasia-disorganized cerebellar cortical architecture I.

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Morrison RS, Kinoshita Y, Johnson MD, Guo W, Garden GA (2003) p53- dependent cell death signaling in neurons.

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Sequence 1 leu arg phe cys cys ser arg Sequence 2 leu gap phe cys cys phe arg 3 Withthisalignmentestablished,wecancompare additional sequences.

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