File:Fragile x inheritance.jpg

From Embryology

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This image represents the inheritance of Fragile X Syndrome when the parents are non-symptomatic. When the mother is a carrier of the fragile X chromosome, each child has a 50% chance of inheritance. Since girls have 2 X chromosomes, they are less likely to display symptoms of Fragile X Syndrome when compared to boys.

Drawn by: Tara Lofthouse (z3290815)

Copyright: Beginning six months after publication, I (z3288827) grant the public the non-exclusive right to copy, distribute, or display the Work under a Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/ and http://creativecommons.org/licenses/by-nc-sa/3.0/legalcode.


Assessment

+ Figure relevant to group project. + Meets student drawn criteria. + Copyright, citation and student disclaimer included. + This figure is very useful for understanding inheritance pattern. + You provide further information in the figure legend, demonstrating peer teaching component.



Note - This image was originally uploaded as part of a student project and may contain inaccuracies in either description or acknowledgements. Students have been advised in writing concerning the reuse of content and may accidentally have misunderstood the original terms of use. If image reuse on this non-commercial educational site infringes your existing copyright, please contact the site editor for immediate removal.




Cite this page: Hill, M.A. (2024, June 21) Embryology Fragile x inheritance.jpg. Retrieved from https://embryology.med.unsw.edu.au/embryology/index.php/File:Fragile_x_inheritance.jpg

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© Dr Mark Hill 2024, UNSW Embryology ISBN: 978 0 7334 2609 4 - UNSW CRICOS Provider Code No. 00098G

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Yi efo/eka'e gwa ebo wo le nyangagi wuncin ye kamina wunga tinya nan

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