The search engine for blood group genes. Predicted Amino Acid Change. Erythrogene v0.7 (22 Dec 2016) -. To cite Erythrogene please use the following publication:. Möller, M., Jöud, M., Storry, J. R., and Olsson, M. L. Erythrogene: a database for in-depth analysis of the extensive variation in 36 blood group systems in the 1000 Genomes Project. Blood Advances. 2016;1(3):240-249. https:/ doi.org/10.1182/bloodadvances.2016001867.
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The search engine for blood group genes. Predicted Amino Acid Change. Erythrogene v0.7 (22 Dec 2016) -. To cite Erythrogene please use the following publication:. Möller, M., Jöud, M., Storry, J. R., and Olsson, M. L. Erythrogene: a database for in-depth analysis of the extensive variation in 36 blood group systems in the 1000 Genomes Project. Blood Advances. 2016;1(3):240-249. https:/ doi.org/10.1182/bloodadvances.2016001867.
Erythrogene: a database for in-depth analysis of the extensive variation in 36 blood group systems in the 1000 Genomes Project | Blood Advances
http://www.bloodadvances.org/content/1/3/240
Skip to main content. Search for this keyword. Search for this keyword. Erythrogene: a database for in-depth analysis of the extensive variation in 36 blood group systems in the 1000 Genomes Project. Doi: https:/ doi.org/10.1182/bloodadvances.2016001867. Hematology and Transfusion Medicine, Department of Laboratory Medicine, Lund University, Lund, Sweden; and. Find this author on Google Scholar. Find this author on PubMed. Search for this author on this site. ORCID record for Mattias Möller. Find this au...
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Initiated 2004 as national registry in Germany (PV-ERY-KA 03) by Holger Cario. Web-based International database developed 2005 by ML. Ribeiro and C. Bento,. Hematology Unit, Centro Hospitalar de Coimbra, Portugal. Prospective registration and data collection of patients with congenital or idiopathic erythrocytosis (priority for patients with defined genetic cause). Characterisation of these diseases by clinical examination, hematological, biochemical, and molecular genetic analyses.
Polycythemias
Initiated 2004 as national registry in Germany (PV-ERY-KA 03) by Holger Cario. Web-based International database developed 2005 by ML. Ribeiro and C. Bento,. Hematology Unit, Centro Hospitalar de Coimbra, Portugal. Prospective registration and data collection of patients with congenital or idiopathic erythrocytosis (priority for patients with defined genetic cause). Characterisation of these diseases by clinical examination, hematological, biochemical, and molecular genetic analyses.
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Erythrogene
The search engine for blood group genes. Predicted Amino Acid Change. Erythrogene v0.7 (22 Dec 2016) -. To cite Erythrogene please use the following publication:. Möller, M., Jöud, M., Storry, J. R., and Olsson, M. L. Erythrogene: a database for in-depth analysis of the extensive variation in 36 blood group systems in the 1000 Genomes Project. Blood Advances. 2016;1(3):240-249. https:/ doi.org/10.1182/bloodadvances.2016001867.
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