| Autor: |
P. J., Sujitha, Gomathi, V. |
| Předmět: |
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| Zdroj: |
Indian Journal of Public Health Research & Development; Jun2020, Vol. 11 Issue 6, p997-1003, 7p |
| Abstrakt: |
There has been a precipitous advancement of unequivocal technological and methodological upgradings in genetics and genomics, thereby allowing to identify atypical mutations that are involved in complex neurodevelopmental conditions. Neoteric advancements in genomics such as whole - exome or whole genome sequencing have endorsed scientist to identify extensive mutations underlying NDDS. In this review we are recapitating the new-fangled developments in genomic analysis and deciphering it into clinical practice. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
| Externí odkaz: |
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