File:Codominant inheritance.jpg: Difference between revisions
(==Codominant Inheritance== The ABO blood group is a major system for classifying blood types in humans. Blood type AB is inherited in a codominant pattern. In this example, a father with blood type A and a mother with blood type B have four children, eac) |
|||
(3 intermediate revisions by 2 users not shown) | |||
Line 1: | Line 1: | ||
==Codominant Inheritance== | ==Codominant Inheritance== | ||
The ABO blood group is a major system for classifying blood types in humans | The ABO blood group is a major system for classifying blood types in humans. | ||
Blood type AB is inherited in a codominant pattern. In this example, a father with blood type A and a mother with blood type B have four children, each with a different blood type: A, AB, B, and O. | |||
'''Links:''' {{spermatozoa}} | {{oocyte}} | {{blood}} | |||
{{GHR Inheritance}} | |||
===Reference=== | |||
Image - Genetics Home Reference. http://ghr.nlm.nih.gov/handbook/illustrations/codominant | |||
====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]] | {{Footer}} | ||
[[Category:Genetics]] [[Category:Meiosis]] [[Category:Blood]] |
Latest revision as of 13:42, 23 July 2018
Codominant Inheritance
The ABO blood group is a major system for classifying blood types in humans.
Blood type AB is inherited in a codominant pattern. In this example, a father with blood type A and a mother with blood type B have four children, each with a different blood type: A, AB, B, and O.
Links: spermatozoa | oocyte | blood
- 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
Reference
Image - Genetics Home Reference. http://ghr.nlm.nih.gov/handbook/illustrations/codominant
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 17) Embryology Codominant inheritance.jpg. Retrieved from https://embryology.med.unsw.edu.au/embryology/index.php/File:Codominant_inheritance.jpg
- © Dr Mark Hill 2024, UNSW Embryology ISBN: 978 0 7334 2609 4 - UNSW CRICOS Provider Code No. 00098G
File history
Yi efo/eka'e gwa ebo wo le nyangagi wuncin ye kamina wunga tinya nan
Gwalagizhi | Nyangagi | Dimensions | User | Comment | |
---|---|---|---|---|---|
current | 09:55, 12 May 2010 | 307 × 396 (65 KB) | S8600021 (talk | contribs) | ==Codominant Inheritance== The ABO blood group is a major system for classifying blood types in humans. Blood type AB is inherited in a codominant pattern. In this example, a father with blood type A and a mother with blood type B have four children, eac |
You cannot overwrite this file.
File usage
The following 13 pages use this file:
- 2010 BGD Practical 3 - Gametogenesis
- 2011 Lab 1 - Gametogenesis
- ANAT2341 Lab 1 - Gametogenesis
- ANAT2341 Lab 3 2013
- Abnormal Development - Genetic
- BGDA Practical 3 - Gametogenesis
- Fetal Cells in Maternal Blood
- Genome Sequencing
- Molecular Development - Genetics
- Non-Invasive Prenatal Testing
- Preimplantation Genetic Diagnosis
- Prenatal Diagnosis
- X chromosome