Facial detection of genetic disorders
<p>An estimated 400,000 children are born every year with rare genetic disorders that significantly affect their quality of life. Early detection and intervention can significantly improve the quality of life of these children. Craniofacial characteristics contain highly useful information for...
Päätekijä: | Alvi, MS |
---|---|
Muut tekijät: | Zisserman, A |
Aineistotyyppi: | Opinnäyte |
Kieli: | English |
Julkaistu: |
2019
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Aiheet: |
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