| dc.contributor.author | Suresh Bhargav, D | |
| dc.contributor.author | Sreedevi, N | |
| dc.contributor.author | Swapna, N | |
| dc.contributor.author | Srinivas, K | |
| dc.date.accessioned | 2025-07-03T10:34:47Z | |
| dc.date.available | 2025-07-03T10:34:47Z | |
| dc.date.issued | 2017 | |
| dc.identifier.uri | http://203.129.241.86:8080/xmlui/handle/123456789/5630 | |
| dc.title | Whole exome sequencing in the molecular diagnosis of microcephaly: A tale of PYCR2 gene and hypomyelinating leukodystrophy-10. | |
| dc.type | Other | |
| dc.namecssw | Indian Society for Human Genetics (ISHG) | |
| dc.place | Bengaluru. | |
| dc.note | Paper presented at the Indian Society for Human Genetics (ISHG) |
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