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http://20.193.157.4:9595/xmlui/handle/123456789/1140Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | DR R.S.BULAGOUDADR G.S.KADAKOL, DR M M PATIL, DR S.V.PATIL, DR BHEEMSHETTY S. PATIL | - |
| dc.date.accessioned | 2019-11-06T07:20:20Z | - |
| dc.date.available | 2019-11-06T07:20:20Z | - |
| dc.date.issued | 2017-04 | - |
| dc.identifier.uri | http://hdl.handle.net/123456789/1140 | - |
| dc.description.abstract | Fragile-X syndrome (FXS) is the most common inherited form of mental disorder. The clinical features of FXS include moderate to severe mental retardation, dysmorphic facial features. One such case was seen & admitted in our hospital with similar clinical symptoms. We examined both clinical and cytological analysis. After examining all these we found child with Fragile X Syndrome. We suggest that molecular analysis of Fragile X Syndrome related to FMR1gene will help to know the novel mutation in this population, which will be helpful for early diagnosis of Fragile-X syndrome and type of genetic disorder. | en_US |
| dc.language.iso | en | en_US |
| dc.publisher | BLDE(Deemed to be University) | en_US |
| dc.subject | Fragile X Syndrome (FXS), Mental retardation, Cytogenetic Analysis, Clinical case Fragile X Syndrome. | en_US |
| dc.title | FRAGILE X SYNDROME: CLINICAL & CYTOLOGICAL STUDY IN NORTH KARNATAKA | en_US |
| dc.type | Article | en_US |
| Appears in Collections: | Faculty of Anatomy | |
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