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| Untersuchte Arbeit: Seite: 87, Zeilen: (21-22).22-26 |
Quelle: Walters et al 2010 Seite(n): 673, Zeilen: left col. 21-25 |
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| Furthermore Walters et al; demonstrated that a 16p11.2 deletion give rise to a strongly-expressed obesity phenotype. Possible explanations include a direct causal relationship between obesity and developmental delay; the involvement of the same or related regulatory pathways; or different outcomes of the same set of behavioural disorders with complex pleiotropic effects and variable ages of onset and expressivities (Walters 2010).
84. Walters R. G. et al. A novel highly-penetrant form of obesity due to microdeletions on chromosome 16p11.2. Nature. 2010 February 4; 463(7281): 671–675 |
Possible explanations include a direct causal relationship between obesity and developmental delay, the involvement of the same or related regulatory pathways, or different outcomes of the same set of behavioural disorders with complex pleiotropic effects and variable ages of onset and expressivities. |
The source is mentioned at the end, but the reader cannot know that this passage has been copied verbatim. |
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