Please use this identifier to cite or link to this item:
http://repo.lib.jfn.ac.lk/ujrr/handle/123456789/7514Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Joseph Anne, D. D. | - |
| dc.contributor.author | Sirisena Nirmala, D. | - |
| dc.contributor.author | Kumanan, T. | - |
| dc.contributor.author | Sujanitha, V. | - |
| dc.date.accessioned | 2022-09-26T05:40:47Z | - |
| dc.date.available | 2022-09-26T05:40:47Z | - |
| dc.date.issued | 2019 | - |
| dc.identifier.citation | 3rd Annual Rare Disease Day Symposium 2019, 28th February 2019 at New Auditorium of Lady Ridgeway Children’s Hospital, Colombo, Sri Lanka. | en_US |
| dc.identifier.uri | http://repo.lib.jfn.ac.lk/ujrr/handle/123456789/7514 | - |
| dc.language.iso | en | en_US |
| dc.publisher | Rare Disease Forum of the Sri Lanka College of Paediatricians | en_US |
| dc.subject | Hypoparathyroidism | en_US |
| dc.subject | Renal disease | en_US |
| dc.subject | Barakat syndrome | en_US |
| dc.subject | Sensorineural deafness | en_US |
| dc.title | A family with hypoparathyroidism, sensorineural deafness and renal disease (Barakat syndrome) caused by a reduced gene dosage in GATA3 | en_US |
| dc.type | Research abstract | en_US |
| Appears in Collections: | Medicine | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| Abstract application form_BS abstract-1 (1).pdf | 336.99 kB | Adobe PDF | ![]() View/Open |
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