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==Mitochondrial Genome Inheritance==
==Mitochondrial Genome Inheritance==


In one family, a woman with a mitochondrial disorder and her unaffected husband have only affected children. In another family, a man with a mitochondrial condition and his unaffected wife have no affected children.
In one family, a woman with a {{mitochondria}}l disorder and her unaffected husband have only affected children. In another family, a man with a mitochondrial condition and his unaffected wife have no affected children.


{{Template:GHR Inheritance}}


'''Links:''' [[Spermatozoa Development|Spermatozoa]] | [[Oocyte Development|Oocyte]]


{{GHR Inheritance}}


'''Source:''' Genetics Home Reference. http://ghr.nlm.nih.gov/handbook/illustrations/mitochondrial


'''Links:''' {{oocyte}} | {{mitochondria}} | {{spermatozoa}}
===Reference===
Genetics Home Reference. http://ghr.nlm.nih.gov/handbook/illustrations/mitochondrial
====Copyright====
Government information at NLM Web sites is in the public domain. Public domain information may be freely distributed and copied, but it is requested that in any subsequent use the National Library of Medicine (NLM) be given appropriate acknowledgement. http://www.nlm.nih.gov/copyright.html
Government information at NLM Web sites is in the public domain. Public domain information may be freely distributed and copied, but it is requested that in any subsequent use the National Library of Medicine (NLM) be given appropriate acknowledgement. http://www.nlm.nih.gov/copyright.html


[[Category:Genetics]] [[Category:Meiosis]] [[Category:Muscle]]
{{Footer}}
[[Category:Genetics]] [[Category:Meiosis]] [[Category:Muscle]][[Category:Mitochondria]]

Latest revision as of 13:39, 23 July 2018

Mitochondrial Genome Inheritance

In one family, a woman with a mitochondrial disorder and her unaffected husband have only affected children. In another family, a man with a mitochondrial condition and his unaffected wife have no affected children.


Inheritance Pattern images: Genetic Abnormalities | autosomal dominant | autosomal recessive | X-linked dominant (affected father) | X-Linked dominant (affected mother) | X-Linked recessive (affected father) | X-Linked recessive (carrier mother) | mitochondrial inheritance | Codominant inheritance | Genogram symbols | Genetics


Links: oocyte | mitochondria | spermatozoa

Reference

Genetics Home Reference. http://ghr.nlm.nih.gov/handbook/illustrations/mitochondrial

Copyright

Government information at NLM Web sites is in the public domain. Public domain information may be freely distributed and copied, but it is requested that in any subsequent use the National Library of Medicine (NLM) be given appropriate acknowledgement. http://www.nlm.nih.gov/copyright.html


Cite this page: Hill, M.A. (2024, May 6) Embryology Mitochondrial inheritance.jpg. Retrieved from https://embryology.med.unsw.edu.au/embryology/index.php/File:Mitochondrial_inheritance.jpg

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

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current08:35, 12 May 2010Thumbnail for version as of 08:35, 12 May 2010307 × 396 (53 KB)S8600021 (talk | contribs)Mitochondrial genome inheritance In one family, a woman with a mitochondrial disorder and her unaffected husband have only affected children. In another family, a man with a mitochondrial condition and his unaffected wife have no affected children. Sour