Osteogenesis imperfecta in Brazilian patients

Autor: Maira Trancozo, Marcos V.D. Moraes, Dalila A. Silva, Jéssica A.M. Soares, Clara Barbirato, Márcio G. Almeida, Lígia R. Santos, Maria R. G. O. Rebouças, Akel N. Akel Jr, Valentim Sipolatti, Vanda R. R. Nunes, Flavia I. V. Errera, Meire Aguena, Maria R. Passos-Bueno, Flavia de Paula

Publikováno v: Genetics and Molecular Biology, Vol 42, Iss 2, Pp 344-350 (2019)

Abstract Osteogenesis Imperfecta (OI) is a heterogeneous genetic disorder characterized by bone fragility and fracture. Mutations in 20 distinct genes can cause OI, and therefore, the genetic diagnosis of OI is frequently difficult to obtain because

Externí odkaz: https://doaj.org/article/dcedd6b038014600a2ab4de446f4d7a9

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Tuning of power plant voltage and reactive power controllers considering equivalent short circuit ratio

Autor: P. Partinen, P. H. Nielsen, O. - P. Janhunen, L. Linnamaa, N. Akel, K. Nayebi, T. Lund, A. Harjula

Publikováno v: 21st Wind & Solar Integration Workshop (WIW 2022).

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::6f40d362ddb952e65b4c02984455093e
https://doi.org/10.1049/icp.2022.2832

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Osteogenesis imperfecta in Brazilian patients

Autor: Meire Aguena, Jéssica A.M. Soares, Clara Barbirato, Márcio G. Almeida, Maria Rita Passos-Bueno, Marcos V.D. Moraes, Maria Regina Galvêas Oliveira Rebouças, Vanda R. R. Nunes, Lígia Ramos dos Santos, Flavia de Paula, Flavia Imbroisi Valle Errera, Maira Trancozo, Valentim Sipolatti, Akel N. Akel, Dalila A. Silva

Publikováno v: Genetics and Molecular Biology v.42 n.2 2019
Genetics and Molecular Biology
Sociedade Brasileira de Genética (SBG)
instacron:SBG
Genetics and Molecular Biology, Vol 42, Iss 2, Pp 344-350 (2019)
Genetics and Molecular Biology, Volume: 42, Issue: 2, Pages: 344-350, Published: 15 AUG 2019
Genetics and Molecular Biology, Issue: ahead, Published: 15 AUG 2019

Osteogenesis Imperfecta (OI) is a heterogeneous genetic disorder characterized by bone fragility and fracture. Mutations in 20 distinct genes can cause OI, and therefore, the genetic diagnosis of OI is frequently difficult to obtain because of the gr

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0dd9ef5b0fad92cb8443609a4d18401c
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572019000300344