Down Syndrome: Development Of A Non-Invasive Prenatal Dna Screening Test Using Superoxide Dismutase 1 Gene In Maternal Blood And Detection Of Cystathionine P-Synthase Gene Mutations
Down syndrome or Trisomy 21, is the most commonly occurring genetic disorder that stems from the failure of ·chromosome 21 to segregate normally during meiosis, resulting in an individual carrying an extra copy of chromosome 21. The main aims of this study were to develop a relatively non-invasiv...
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| Aineistotyyppi: | Opinnäyte |
| Kieli: | English English |
| Julkaistu: |
2004
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| Linkit: | http://psasir.upm.edu.my/id/eprint/6578/1/FPSK%28P%29_2004_7.pdf |
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