PAFAH1B1/Related Articles

See also changes related to PAFAH1B1, or pages that link to PAFAH1B1 or to this page or whose text contains "PAFAH1B1".

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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]

Other related topics

• 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]

Articles related by keyphrases (Bot populated)

• Pachygyria [r]: A congenital malformation of the cerebral hemisphere that results in unusually thick convolutions of the cerebral cortex. ^[e]
• Luteinising hormone [r]: Pituitary hormone with an essential role in reproduction in both males and females. ^[e]
• Lissencephalic [r]: Add brief definition or description