Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Lima, Naynne Soares de"'
Autor:
Lima, Naynne Soares de, Gomes, Luana Ferreira, Oliveira, Beatriz Reis de, Oliveira, Victória Rocha de, Oliveira, Ilzver de Matos
Publikováno v:
Research, Society and Development; Vol. 10 No. 11; e433101119924
Research, Society and Development; Vol. 10 Núm. 11; e433101119924
Research, Society and Development; v. 10 n. 11; e433101119924
Research, Society and Development
Universidade Federal de Itajubá (UNIFEI)
instacron:UNIFEI
Research, Society and Development; Vol. 10 Núm. 11; e433101119924
Research, Society and Development; v. 10 n. 11; e433101119924
Research, Society and Development
Universidade Federal de Itajubá (UNIFEI)
instacron:UNIFEI
There is a problem or an increase in the incarcerated population and the consequences related to social inequality for institutions that develop social policies as a way to improve living conditions in prison. In relation to health conditions, or the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3056::0333214401e51793662a5e09b4264633
https://rsdjournal.org/index.php/rsd/article/view/19924
https://rsdjournal.org/index.php/rsd/article/view/19924
Autor:
Gomes, Luana Ferreira, Oliveira, Beatriz Reis de, Lima, Naynne Soares de, Oliveira, Victória Rocha de, Santana, Ellen Maiany Ribeiro, Vasconcellos, Sara Juliana de Abreu de, Barros, Alina Lúcia de Oliveira, Macedo, Álvaro Bezerra
Publikováno v:
Research, Society and Development; Vol. 10 No. 11; e190101119531
Research, Society and Development; Vol. 10 Núm. 11; e190101119531
Research, Society and Development; v. 10 n. 11; e190101119531
Research, Society and Development
Universidade Federal de Itajubá (UNIFEI)
instacron:UNIFEI
Research, Society and Development; Vol. 10 Núm. 11; e190101119531
Research, Society and Development; v. 10 n. 11; e190101119531
Research, Society and Development
Universidade Federal de Itajubá (UNIFEI)
instacron:UNIFEI
Cornelia de Lange syndrome (CLS) is a rare genetic disease with an estimated prevalence of 1 in every 30,000 live births. The main features are distinct craniofacial disorders, abnormalities in the upper and lower limbs and intellectual deficit, vary
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3056::5c2ae4d049f9032534d72e0a19b7a8c7
https://rsdjournal.org/index.php/rsd/article/view/19531
https://rsdjournal.org/index.php/rsd/article/view/19531