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dc.contributor.authorGiugliani, Robertopt_BR
dc.contributor.authorBender, Fernandapt_BR
dc.contributor.authorCouto, Rowena Rubim Silva dopt_BR
dc.contributor.authorBochernitsan, Aline Nemetzpt_BR
dc.contributor.authorFacchin, Ana Carolina Brusiuspt_BR
dc.contributor.authorBurin, Maira Graeffpt_BR
dc.contributor.authorAmorim, Tatianapt_BR
dc.contributor.authorAcosta, Angelina Xavierpt_BR
dc.contributor.authorPurificação, Antônio Conceição dapt_BR
dc.contributor.authorLeistner-Segal, Sandrapt_BR
dc.contributor.authorPereira, Maria Luiza Saraivapt_BR
dc.contributor.authorJardim, Laura Bannachpt_BR
dc.contributor.authorMatte, Ursula da Silveirapt_BR
dc.contributor.authorRiegel, Marilucept_BR
dc.contributor.authorSantos, Augusto César Cardoso dospt_BR
dc.contributor.authorRodrigues, Graziella Ramospt_BR
dc.contributor.authorOliveira, Marcelo Zagonel dept_BR
dc.contributor.authorRibeiro, Alice Taglianipt_BR
dc.contributor.authorHeck, Selia Mariapt_BR
dc.contributor.authorDresch, Vanusapt_BR
dc.contributor.authorFaccini, Lavinia Schulerpt_BR
dc.contributor.authorKubaski, Francynept_BR
dc.date.accessioned2019-09-27T03:45:07Zpt_BR
dc.date.issued2019pt_BR
dc.identifier.issn1415-4757pt_BR
dc.identifier.urihttp://hdl.handle.net/10183/199807pt_BR
dc.description.abstractRare genetic disorders are currently in the spotlight due to the elevated number of different conditions and significant total number of affected patients. The study of these disorders is extremely helpful for the elucidation of physiological processes related with complex disorders. Isolated populations are instrumental for the study of genetic disorders, considering their homogeneity and high proportion of affected patients in a small geographic area. These favorable conditions lead to the creation of a new discipline, known as "population medical genetics", which integrates medical genetics, population genetics, epidemiological genetics and community genetics. In order to develop practical activities in this new discipline, the National Institute of Population Medical Genetics (INaGeMP) was created in 2008 in Brazil. INaGeMP has developed several tools and funded numerous research activities. In this review, we highlight three successful projects developed in the first 10 years of INaGeMP activities (2008-2018): a newborn screening pilot study for MPS VI in Northeast Brazil, the study of Machado-Joseph disease in Brazilian families with Azorian ancestry, and the high twinning rate in a small town in southern Brazil. The results of these projects in terms of scientific output and contributions to the affected communities highlight the success and importance of INaGeMP.en
dc.format.mimetypeapplication/pdfpt_BR
dc.language.isoengpt_BR
dc.relation.ispartofGenetics and molecular biology. Ribeirão Preto. Vol. 42, n. 1, suppl. 1 (2019), p. 312-320pt_BR
dc.rightsOpen Accessen
dc.subjectGenéticapt_BR
dc.subjectPopulation Medical Geneticsen
dc.subjectgenetic clustersen
dc.subjectGenética médicapt_BR
dc.subjectEstatística e dados numéricospt_BR
dc.subjectfounder effecten
dc.subjectpopulation isolatesen
dc.subjectMétodospt_BR
dc.subjectMapeamento cromossomicopt_BR
dc.subjectDoenças genéticas inataspt_BR
dc.subjectFisiopatologiapt_BR
dc.subjectEpidemiologiapt_BR
dc.subjectDiagnósticopt_BR
dc.subjectTerapêuticapt_BR
dc.titlePopulation medical genetics : translating science to the communitypt_BR
dc.typeArtigo de periódicopt_BR
dc.identifier.nrb001100682pt_BR
dc.type.originNacionalpt_BR


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