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| Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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| 1 |
Material Type: magazinearticle
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The study of copy number variations in the regions of PRKAB2 and PPM1K among congenital heart defects patientsRevista da Associacao Medica Brasileira (1992), 2019-06, Vol.65 (6), p.786-790 [Peer Reviewed Journal]This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License. ;ISSN: 0104-4230 ;ISSN: 1806-9282 ;EISSN: 1806-9282 ;DOI: 10.1590/1806-9282.65.6.786 ;PMID: 31340305Digital Resources/Online E-Resources |
| 2 |
Material Type: magazinearticle
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Síndrome de deleção 22q11 e cardiopatias congênitas complexasRevista da Associação Médica Brasileira, 2011-01, Vol.57 (1), p.62-65 [Peer Reviewed Journal]2011 Elsevier Editora Ltda. and Brazilian Medical Association ;This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License. ;ISSN: 0104-4230 ;ISSN: 1806-9282 ;DOI: 10.1590/S0104-42302011000100018Digital Resources/Online E-Resources |
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- Cromossomos Humanos Par 22 (1)
- Genetic Variation (1)
- Dna Copy Number Variations (1)
- Chromosomes, Human, Pair 22 (1)
- Life Sciences & Biomedicine (1)
- Heart Septal Defects, Ventricular - Genetics (1)
- Case-Control Studies (1)
- Cardiopatias Congêni Tas (1)
- Heart Defects, Congenital (1)
- Digeorge Syndrome (1)
- Chromosome Mapping (1)
- Hibridização In Situ Fluorescente (1)
- Amp-Activated Protein Kinases - Genetics (1)
- Fluorescence (1)
- General & Internal Medicine (1)
- Humans (1)
- Heart Septal Defects (1)
- Genetic Association Studies (1)
- In Situ Hybridization (1)
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