Found: 11
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First molecular identification of mosquito vectors of Dirofilaria immitis in continental Portugal.
- Published in:
- Parasites & Vectors, 2015, v. 8, n. 1, p. 1, doi. 10.1186/s13071-015-0760-2
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- Publication type:
- Article
Variant Rett syndrome in a girl with a pericentric X-chromosome inversion leading to epigenetic changes and overexpression of the MECP2 gene.
- Published in:
- International Journal of Developmental Neuroscience, 2015, v. 46, p. 82, doi. 10.1016/j.ijdevneu.2015.07.010
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- Publication type:
- Article
First seizure as late presentation of velo-cardio-facial syndrome.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2013, v. 26, n. 3/4, p. 381, doi. 10.1515/jpem-2012-0348
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- Publication type:
- Article
The neurobiological basis of psycho-oncology.
- Published in:
- 2016
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- Publication type:
- Editorial
Molecular characterization of a rare analphoid supernumerary marker chromosome derived from 7q35→ qter: a case report.
- Published in:
- Molecular Cytogenetics (17558166), 2016, v. 9, p. 1, doi. 10.1186/s13039-016-0295-z
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- Publication type:
- Article
Electrochemically Mediated Atom Transfer Radical Polymerization Driven by Alternating Current.
- Published in:
- Angewandte Chemie International Edition, 2024, v. 63, n. 29, p. 1, doi. 10.1002/anie.202406484
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- Publication type:
- Article
Electrochemically Mediated Atom Transfer Radical Polymerization Driven by Alternating Current.
- Published in:
- Angewandte Chemie, 2024, v. 136, n. 29, p. 1, doi. 10.1002/ange.202406484
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- Publication type:
- Article
LAMA2 gene mutation update: Toward a more comprehensive picture of the laminin‐α2 variome and its related phenotypes.
- Published in:
- Human Mutation, 2018, v. 39, n. 10, p. 1314, doi. 10.1002/humu.23599
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- Publication type:
- Article
Efeitos do treino orientado para a tarefa na marcha, equilíbrio e medo de cair após acidente vascular cerebral: estudo de caso.
- Published in:
- Saúde & Tecnologia, 2019, n. 22, p. 28
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- Publication type:
- Article
BRCA1 VUS: A functional analysis to differentiate pathogenic from benign variants identified in clinical diagnostic panels for breast cancer.
- Published in:
- Molecular Medicine Reports, 2023, v. 28, n. 1, p. N.PAG, doi. 10.3892/mmr.2023.13023
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- Publication type:
- Article
Mutations in the MECP2 Gene Are Not a Major Cause of Rett Syndrome-Like or Related Neurodevelopmental Phenotype in Male PatientS.
- Published in:
- Journal of Child Neurology, 2009, v. 24, n. 1, p. 49, doi. 10.1177/0883073808321043
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- Publication type:
- Article