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Autosomal Recessive Inheritance
==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.
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.
{{Template:GHR Inheritance}}
'''Links:''' [[Spermatozoa Development|Spermatozoa]] | [[Oocyte Development|Oocyte]]


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

Revision as of 10:07, 12 May 2010

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.

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


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

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

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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