Prenatal Genome-Wide Sequencing analysis (Exome or Genome) in detecting pathogenic Single Nucleotide Variants in fetal Central Nervous System Anomalies: systematic review and meta-analysis
PediatriaSobre o estudo
- Desenho
- Metanálise
- Nível de evidência
- 1 · Evidência consolidada
- Revista
- European journal of human genetics : EJHG
- Publicado em
- 15 mar 2024
- Citações
- 10
O resumo deste estudo é do publisher e não tem licença aberta: por isso mostramos aqui só os dados do estudo, e o texto fica na fonte original, nos links abaixo.
O estudo original
Prenatal Genome-Wide Sequencing analysis (Exome or Genome) in detecting pathogenic Single Nucleotide Variants in fetal Central Nervous System Anomalies: systematic review and meta-analysis
Enrica Marchionni, Daniele Guadagnolo, Gioia Mastromoro, Antonio Pizzuti
Descritores MeSH
- Polymorphism, Single Nucleotide
- Prenatal Diagnosis
- Central Nervous System
- Female
- Fetus
- Genetic Testing
- Humans
- Nervous System Malformations
- Pregnancy
- Whole Genome Sequencing
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