Uploads by Z3389343
From Embryology
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Date | Name | Thumbnail | Size | Description | Versions |
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18:52, 17 September 2011 | Location of the frataxin gene on chromosome 9.doc (file) | 140 KB | Human chromosome 9, showing the location of the frataxin gene. {{Template:2011 Student Image}} | 1 | |
19:07, 17 September 2011 | The frataxin gene on chromosome 9.jpg (file) | 40 KB | Human Chromosome 9, showing the location of the frataxin gene. {{Template:2011 Student Image}} | 1 | |
19:19, 17 September 2011 | Friedreich's Ataxia Pedigree.jpg (file) | 80 KB | The pedigree of a family affected by Friedreich's Ataxia. Due to the anticipating nature of the inheritance, the severity of symptoms increases while the age of onset decreases with each generation. Heterozygous individuals who possess one allele with the | 1 | |
16:42, 10 October 2011 | Friedreich's Ataxia Pedigree.png (file) | 58 KB | The pedigree of a family affected by Friedreich's Ataxia. Due to the anticipating nature of the inheritance, the severity of symptoms increases while the age of onset decreases with each generation. Heterozygous individuals who possess one allele with the | 1 | |
16:25, 12 October 2011 | Location of the frataxin gene on chromosome 9.jpg (file) | 13 KB | Cytogenetic Location: 9q21.11 Molecular Location on chromosome 9: base pairs 71,650,478 to 71,715,093 The FXN gene is located on the long (q) arm of chromosome 9 at position 21.11. More precisely, the FXN gene is located from base pair 71,650,478 to base | 1 | |
11:46, 13 October 2011 | Pedigree of Friedreich's Ataxia.PNG (file) | 46 KB | The pedigree of a family affected by Friedreich's Ataxia. Due to the anticipating nature of the inheritance, the severity of symptoms increases while the age of onset decreases with each generation. Heterozygous individuals who possess one allele with the | 1 |