PAFAH1B1/Related Articles: Difference between revisions
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Revision as of 15:41, 3 August 2009
- See also changes related to PAFAH1B1, or pages that link to PAFAH1B1 or to this page or whose text contains "PAFAH1B1".
Parent topics
- Gene [r]: The functional unit of heredity. [e]
- Brain [r]: The core unit of a central nervous system. [e]
- Brain development [r]: The build-up of the brain from ectodermal cells to a complex structure of neurons, glia and blood vessels. [e]
Subtopics
- Lissencephaly [r]: Condition in which the cortical surface is smooth, as opposed to gyrified. Normal in many mammals and transient in human fetal development but a disorder in humans born with it. [e]
- Neuronal migration [r]: The process by which nerve cells travel from the place of their last cell division to their final position in the brain. [e]
- Gyrification [r]: The folding process during brain development, or the extent of folding. [e]
- Polymicrogyria [r]: A disorder in which the cortical surface resembles that of a road paved with cobblestones. [e]