File:Autosomal recessive inheritance.jpg: Difference between revisions

From Embryology
No edit summary
mNo edit summary
Line 3: Line 3:
In this example, two unaffected parents each carry one copy of a gene mutation for an autosomal recessive disorder. They have one affected child and three unaffected children, two of which carry one copy of the gene mutation.
In this example, two unaffected parents each carry one copy of a gene mutation for an autosomal recessive disorder. They have one affected child and three unaffected children, two of which carry one copy of the gene mutation.


===Examples of Autosomal Dominant Disease===


{{Template:GHR Inheritance}}
* '''Cystic fibrosis''' (CF)


* '''Sickle cell anaemia''' {{blood}}


:'''Links:''' [[Spermatozoa Development|Spermatozoa]] | [[Oocyte Development|Oocyte]] | [http://www.ncbi.nlm.nih.gov/sites/entrez?db=pubmed&cmd=search&term=autosomal_inheritance Search Pubmed - autosomal inheritance]
* '''Tay-Sachs disease'''




{{GHR Inheritance}}




----
:'''Links:''' [[Spermatozoa Development|Spermatozoa]] | [[Oocyte Development|Oocyte]] | [http://www.ncbi.nlm.nih.gov/sites/entrez?db=pubmed&cmd=search&term=autosomal_inheritance Search Pubmed - autosomal inheritance]
===Reference===


Source: Genetics Home Reference. http://ghr.nlm.nih.gov/handbook/illustrations/autorecessive
Image Source: Genetics Home Reference. http://ghr.nlm.nih.gov/handbook/illustrations/autorecessive


====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


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

Revision as of 10:57, 23 July 2018

Autosomal Recessive Inheritance

In this example, two unaffected parents each carry one copy of a gene mutation for an autosomal recessive disorder. They have one affected child and three unaffected children, two of which carry one copy of the gene mutation.

Examples of Autosomal Dominant Disease

  • Cystic fibrosis (CF)
  • Sickle cell anaemia blood
  • Tay-Sachs disease


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: Spermatozoa | Oocyte | Search Pubmed - autosomal inheritance

Reference

Image Source: Genetics Home Reference. http://ghr.nlm.nih.gov/handbook/illustrations/autorecessive

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, April 24) Embryology Autosomal recessive inheritance.jpg. Retrieved from https://embryology.med.unsw.edu.au/embryology/index.php/File:Autosomal_recessive_inheritance.jpg

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

File history

Click on a date/time to view the file as it appeared at that time.

Date/TimeThumbnailDimensionsUserComment
current09:43, 12 May 2010Thumbnail for version as of 09:43, 12 May 2010307 × 396 (65 KB)S8600021 (talk | contribs)Autosomal Recessive Inheritance In this example, two unaffected parents each carry one copy of a gene mutation for an autosomal recessive disorder. They have one affected child and three unaffected children, two of which carry one copy of the gene mutati