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Mostrando ítems 11-20 de 32
Variação morfométrica e citogenética em Kerodon rupestris (Wied, 1820) (Rodentia: Caviidae)
(Universidade Federal do Rio de JaneiroBrasilMuseu NacionalPrograma de Pós-Graduação em Ciências Biológicas (Zoologia)UFRJ, 2017)
Prenatal detection of congenital anomalies and related factors in Argentina
(Springer, 2020-07)
Congenital anomalies (CAs) are a leading cause of neonatal death. Many CAs can be diagnosed prenatally. To estimate the prenatal detection rate (PDR) of CA in hospitals participating in the RENAC (National Network of ...
Divergência genômica e filogeografia de traíras Hoplias malabaricus (Bloch, 1794) (Teleostei: Erythrinidae) na costa leste do BrasilGenomic divergence and phylogeography in trahira Hoplias malabaricus (Bloch, 1794) (Teleostei: Erythrinidae) on Brazilian eastern costal basins
(Universidade Federal de Viçosa, 2017)
Esquizofrenia e síndrome da deleção 22q11.2: Caracterização de genes relevantes
(Universidade Federal de São Paulo (UNIFESP), 2011-02-22)
Introdução: A esquizofrenia é o transtorno mental mais grave e incapacitante entre os distúrbios psiquiátricos. Ela é uma doença complexa e com fenótipo heterogêneo. Dentre os fatores genéticos que parecem ter um papel na ...
A Novel Anti-Mullerian Hormone (AMH) Gene Mutation in a Patient with Persistent Müllerian Duct Syndrome (PMDS) type 1
(Karger, 2019)
PMDS is an autosomic recessive disorder of sexual development caused by inactivating mutations in the AMH or the AMH receptor gene (PMDS type I and II respectively). This condition leads to the persistence of Müllerian ...
Multi-institutional experience of genetic diagnosis in Ecuador: national registry of chromosome alterations and polymorphisms
(2020)
Background: Detection of chromosomal abnormalities is crucial in various medical areas; to diagnose birth defects, genetic disorders, and infertility, among other complex phenotypes, in individuals across a wide range of ...
Ring-20-syndrome and loss of telomeric regions
(2011)
Background The non-nucleoside reverse transcriptase inhibitor (NNRTI), rilpivirine (TMC278; Tibotec Pharmaceuticals, County Cork, Ireland), had equivalent sustained efficacy to efavirenz in a phase 2b trial in treatment-naive ...