Showing 1 - 20 results of 34 for search 'Maria Teresa Vieira Sanseverino', query time: 0.30s Refine Results
  1. 1
    Why are Birth Defects Surveillance Programs Important?
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  2. 2
    Expression profiles of meiotic genes in male vs. female gonads and gametes: Insights into fertility issues
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  3. 3
    A Genética na Fibrose Cística
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  4. 4
    Thalidomide Analogs in Brazil: Concern About Teratogenesis / Análogos da Talidomida no Brasil: Preocupação com a Teratogênese
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  5. 5
    Exposure to misoprostol and hormones during pregnancy and risk of congenital anomalies Exposição ao misoprostol e hormônios durante a gravidez e risco de anomalia congênita
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  6. 6
    Thalidomide Analogs in Brazil: Concern About Teratogenesis
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  7. 7
    Thalidomide Analogs in Brazil: Concern About Teratogenesis
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  8. 8
    Revealing the expression profile of genes that encode the Subcortical Maternal Complex in human reproductive failures
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  9. 9
    Editorial: Teratogenesis: Experimental Models, Mechanisms and Clinical Findings in Humans
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  10. 10
    Reproductive outcomes in an area adjacent to a petrochemical plant in southern Brazil Riscos reprodutivos em região próxima ao pólo petroquímico de Triunfo no Sul do Brasil
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  11. 11
    Reproductive outcomes in an area adjacent to a petrochemical plant in southern Brazil
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  12. 12
    High-risk twin pregnancy: case report of an adolescent patient with cystic fibrosis and systemic lupus erythematosus
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  13. 13
    COVID-19 during pregnancy and adverse outcomes: Concerns and recommendations from The Brazilian Teratology Information Service
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  14. 14
    Epileptic encephalopathy and atypical Rett syndrome with mutations in CDKL5: clinical and molecular characterization of two Brazilian patients
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  15. 15
    The natural history of pregnancies with prenatal diagnosis of Trisomy 18 or Trisomy 13: Retrospective cases of a 23-year experience in a Brazilian public hospital
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  16. 16
    Epileptic encephalopathy and atypical Rett syndrome with mutations in CDKL5: clinical and molecular characterization of two Brazilian patients Encefalopatia epilética e síndrome de Rett atípica por mutações no gene CDKL5: caracterização clínica e molecular de dois casos brasileiros
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  17. 17
    The role of ESCO2, SALL4 and TBX5 genes in the susceptibility to thalidomide teratogenesis
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  18. 18
    [PROVISIONAL] Determining the Pathogenicity of CFTR Missense Variants: Multiple Comparison of in silico Predictors and Variant Annotation Databases
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  19. 19
    Prevalence of thrombophilia-associated genetic risk factors in blood donors of a regional hospital in southern Brazil
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  20. 20
    Diagnóstico pré-natal
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