Copy number variations on chromosome 15 detected by molecular karyotyping in patients with developmental delay and congenital anomalies
Introduction: Global developmental delay (GDD) and congenital anomalies represent a heterogeneous group of medical conditions that may have a known genetic etiology. Molecular karyotyping is the gold standard for detecting copy number variations (CNV), and the first-line test in patients with GDD an...
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| 主要な著者: | , , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
University of Belgrade, Medical Faculty
2023-01-01
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| シリーズ: | Medicinski Podmladak |
| 主題: | |
| オンライン･アクセス: | https://scindeks-clanci.ceon.rs/data/pdf/0369-1527/2023/0369-15272305043B.pdf |
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