File:Prader-Willi Syndrome patient.png

Photograph of a Prader-Willi Syndrome patient

A 12 year old Prader Willi Syndrome patient with the common characteristic of obesity

Reference

FRIDMAN, Cintia and KOIFFMANN, Célia P.. Genomic imprinting: genetic mechanisms and phenotypic consequences in Prader-Willi and Angelman syndromes. Genet. Mol. Biol. [online]. 2000, vol.23, n.4, pp. 715-724 . Available from: <http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572000000400004&lng=en&nrm=iso>. ISSN 1415-4757. http://dx.doi.org/10.1590/S1415-47572000000400004

This paper is not available in Pubmed

Copyright

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Assessment

+ Very relevant to group project topic. + Includes copyright information and and student disclaimer. + Legend includes some description of image. - I would have preferred an image from a PubMed available research or review article.

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, April 26) Embryology Prader-Willi Syndrome patient.png. Retrieved from https://embryology.med.unsw.edu.au/embryology/index.php/File:Prader-Willi_Syndrome_patient.png

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