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In this example, an unaffected woman carries one copy of a gene mutation for an X-linked recessive disorder. She has an affected son, an unaffected daughter who carries one copy of the mutation, and two unaffected children who do not have the mutation.
In this example, an unaffected woman carries one copy of a gene mutation for an X-linked recessive disorder. She has an affected son, an unaffected daughter who carries one copy of the mutation, and two unaffected children who do not have the mutation.


{{Template:GHR Inheritance}}
{{GHR Inheritance}}


'''Links:''' [[Spermatozoa Development|Spermatozoa]] | [[Oocyte Development|Oocyte]]
'''Links:''' [[Musculoskeletal_System_-_Abnormalities#Duchenne_Muscular_Dystrophy|Duchenne Muscular Dystrophy]] | [[Spermatozoa Development|Spermatozoa]] | [[Oocyte Development|Oocyte]]




Source: Genetics Home Reference. http://ghr.nlm.nih.gov/handbook/illustrations/xlinkrecessivemother
===Reference===
 
Genetics Home Reference. http://ghr.nlm.nih.gov/handbook/illustrations/xlinkrecessivemother
 
====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]]

Latest revision as of 10:43, 16 September 2016

X-Linked recessive (carrier mother)

In this example, an unaffected woman carries one copy of a gene mutation for an X-linked recessive disorder. She has an affected son, an unaffected daughter who carries one copy of the mutation, and two unaffected children who do not have the 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: Duchenne Muscular Dystrophy | Spermatozoa | Oocyte


Reference

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

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, June 1) Embryology X-Linked recessive (carrier mother).jpg. Retrieved from https://embryology.med.unsw.edu.au/embryology/index.php/File:X-Linked_recessive_(carrier_mother).jpg

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

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