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==X-Linked recessive (affected father)== | ==X-Linked recessive (affected father)== | ||
In this example, a man with an X-linked recessive condition has two unaffected daughters who each carry one copy of the gene mutation, and two unaffected sons who do not have the mutation. | |||
{{Template:GHR Inheritance}} | |||
'''Links:''' [[Spermatozoa Development|Spermatozoa]] | [[Oocyte Development|Oocyte]] | |||
Source: Genetics Home Reference. http://ghr.nlm.nih.gov/handbook/illustrations/xlinkrecessivefather | Source: Genetics Home Reference. http://ghr.nlm.nih.gov/handbook/illustrations/xlinkrecessivefather |
Revision as of 10:08, 12 May 2010
X-Linked recessive (affected father)
In this example, a man with an X-linked recessive condition has two unaffected daughters who each carry one copy of the gene mutation, and two unaffected sons 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: Spermatozoa | Oocyte
Source: Genetics Home Reference. http://ghr.nlm.nih.gov/handbook/illustrations/xlinkrecessivefather
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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- 2010 BGD Practical 3 - Gametogenesis
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- Abnormal Development - Genetic
- BGDA Lecture - Development of the Nervous System
- BGDA Practical 3 - Gametogenesis
- Fetal Cells in Maternal Blood
- Fragile X Syndrome
- Genome Sequencing
- Human Abnormal Development
- Molecular Development - Genetics
- Non-Invasive Prenatal Testing
- Preimplantation Genetic Diagnosis
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- X Chromosome
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