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      Cytogenetic Investigation in 136 Consecutive Stillbirths: Does the Tissue Type Affect the Success Rate of Chromosomal Microarray Analysis and Karyotype?

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          Abstract

          Chromosomal anomalies are a recognized cause of stillbirth, accounting for 6-17% of the cases. As a diagnostic laboratory method in this setting, conventional karyotyping has two main drawbacks: the need for viable fetal cells in a dead fetus and its limited resolution as compared to alternative techniques.

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          Author and article information

          Journal
          Fetal Diagn Ther
          Fetal diagnosis and therapy
          S. Karger AG
          1421-9964
          1015-3837
          2020
          : 47
          : 4
          Affiliations
          [1 ] Barcelona Center for Fetal and Neonatal Medicine (BCNatal), Hospital Clínic Barcelona, Barcelona, Spain.
          [2 ] Biomedical Diagnostic Center, Hospital Clínic Barcelona, Barcelona, Spain.
          [3 ] Barcelona Center for Fetal and Neonatal Medicine (BCNatal), Hospital Clínic Barcelona, Barcelona, Spain, aborrell@clinic.cat.
          Article
          000505399
          10.1159/000505399
          31955157
          4328a289-b8c4-414c-8324-b4f270d0cb52
          © 2020 S. Karger AG, Basel.
          History

          Chromosomal abnormalities,Chromosomal microarray analysis,Copy number variants,Fetal karyotype,Genetic counselling,Intrauterine death,Prenatal diagnosis,Stillbirth

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