FinDis - Home
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Järjestöjen yhteistyötä harvinaisten sairaus- ja vammaryhmien hyväksi. Harvinaiset-verkosto, Iso Roobertinkatu 20 - 22 A, 5.
How to view the Genealogy files. Leave a comment on How to view the Genealogy files. My Great grandfather Matt August Kaisass Kultala. Amalia Aliina was born Marie Amalia Pettersdtr Ruicka on 15 AUG 1871 in Hietala Simo Finland and died 03 JUN 1917 in Tower Minnesota. This is Grandpa Gust! Leave .
Epidemiological and Clinical Finnish Sample Collections. In these pages we have collected information on epidemiological and clinical Finnish study collections with available DNA samples. Though the list is not comprehensive. The pages include short description of the projects, contact information, as well as information on genome-wide SNP genotyping studies. Link to Studies Summary Table. Link to Studies GWAS Table. In these web pages the .
Welcome to Near East University Genetic Mutation Database. Is a unique resource providing online repository on human inherited disorders mainly people who live in North Cyprus. Innovation and Information Technologies Center.
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I discovered that findis.org is utilizing the Apache/2.2.22 (Ubuntu) os.PAGE TITLE
FinDis - HomeDESCRIPTION
Is a centralized resource for cross-referenced information on disease mutations enriched in the Finnish population. FinDis provides up-to-date information on the 36 monogenic diseases belonging to the Finnish disease heritage. For each disease, this resource provides. Prevalence or incidence and a short description of clinical symptoms. Genetic locus and a molecular description for identified mutations. Disease allele frequencies typically reported for Finnish mutations. Read About the FinDis project.CONTENT
This domain has the following in the web page, "Is a centralized resource for cross-referenced information on disease mutations enriched in the Finnish population." We observed that the web page also stated " FinDis provides up-to-date information on the 36 monogenic diseases belonging to the Finnish disease heritage." It also stated " For each disease, this resource provides. Prevalence or incidence and a short description of clinical symptoms. Genetic locus and a molecular description for identified mutations. Disease allele frequencies typically reported for Finnish mutations. Read About the FinDis project."VIEW MORE WEB PAGES
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