File:Schematic diagram detailing genes deleted in probands.jpeg: Difference between revisions
(Original file name: pone.0012349.s007.tif Schematic diagrams detailing genes deleted in probands. The red box on each diagram represents the affected region. The LCR-mediated, typical WS deleted region is shown in yellow on A and B. The RefSeq and sno/mi) |
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'''Reference''' | '''Reference''' | ||
Ariel M. Pani et al ‘’’ Genome Rearrangements Detected by SNP Microarrays in Individuals with Intellectual Disability Referred with Possible Williams Syndrome.’’’ PLoS ONE: 2010, 5(8);e12349 PMID: | Ariel M. Pani et al ‘’’ Genome Rearrangements Detected by SNP Microarrays in Individuals with Intellectual Disability Referred with Possible Williams Syndrome.’’’ PLoS ONE: 2010, 5(8);e12349 PMID: 20824207 | ||
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Copyright Pani et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. | Copyright Pani et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. | ||
{{Template:2011 Student Image} | {{Template:2011 Student Image}} | ||
Latest revision as of 20:42, 4 October 2011
Original file name: pone.0012349.s007.tif
Schematic diagrams detailing genes deleted in probands. The red box on each diagram represents the affected region. The LCR-mediated, typical WS deleted region is shown in yellow on A and B. The RefSeq and sno/miRNA genes deleted for each proband are shown. Diagrams were adapted from UCSC Genome Browser [26]. (A,B) Genes affected on chromosome 7 including all or part of the WS typical region for probands (A) 8399, (B) 9164, 9061, 9101 and 9152. (C) Genes impacted by the deletion (red) and inversion (grey) on chromosome 5 of proband 9101. Note the disruption of CDH10 at the inversion junction. (D) Deletion on chromosome 1 of proband 9164 impacting 10 RefSeq genes.
Reference
Ariel M. Pani et al ‘’’ Genome Rearrangements Detected by SNP Microarrays in Individuals with Intellectual Disability Referred with Possible Williams Syndrome.’’’ PLoS ONE: 2010, 5(8);e12349 PMID: 20824207
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2930846/#pone.0012349.s007
Copyright Pani et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
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Cite this page: Hill, M.A. (2024, April 18) Embryology Schematic diagram detailing genes deleted in probands.jpeg. Retrieved from https://embryology.med.unsw.edu.au/embryology/index.php/File:Schematic_diagram_detailing_genes_deleted_in_probands.jpeg
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