| 000 | 01716cam a2200349 a 4500 | ||
|---|---|---|---|
| 003 | EG-GiCUC | ||
| 005 | 20250223030751.0 | ||
| 008 | 130216s2012 ua d f m 000 0 eng d | ||
| 040 |
_aEG-GiCUC _beng _cEG-GiCUC |
||
| 041 | 0 | _aeng | |
| 049 | _aDeposite | ||
| 097 | _aPh.D | ||
| 099 | _aCai01.11.12.Ph.D.2012.Mo.C | ||
| 100 | 0 | _aMona Ahmed Elakkad | |
| 245 | 1 | 0 |
_aConnexin 26 gene in non-syndromic hearing loss / _cMona Ahmed Elakkad ; Supervised Ahmad Sameh Farid , Mohamed Ibrahim Shabana , Maha Hassan AbouElew |
| 246 | 1 | 5 | _aضعف السمع الغير متلازم و الجين كونكسين ٢٦ |
| 260 |
_aCairo : _bMona Ahmed Elakkad , _c2012 |
||
| 300 |
_a111 P. : _bcharts ; _c25cm |
||
| 502 | _aThesis (Ph.D.) - Cairo University - Faculty of Medicine - Department of E.N.T | ||
| 520 | _aMutations in GJB2 gene, encoding the gap-junction protein connexion 26 (Cx26) are the leading cause of deafness in autosomal recessive nonsyndromic sensorineural hearing loss (ARNSHL) and the 35delG mutation is the most common in many ethnic groups. To evaluate the extent of contribution of the 35delG mutation of GJB2 gene to ARNSHL in the Egyptian population as well as to correlate the clinical relevance of this mutation to the severity of hearing loss HL | ||
| 530 | _aIssued also as CD | ||
| 653 | 4 | _aConnexin 26 | |
| 653 | 4 | _aGJB2 | |
| 653 | 4 | _aNonsyndromic autosomal recessive sensorineural hearing loss | |
| 700 | 0 |
_aAhmad Sameh Farid , _eSupervisor |
|
| 700 | 0 |
_aMaha Hassan AbouElew , _eSupervisor |
|
| 700 | 0 |
_aMohamed Ibrahim Shabana , _eSupervisor |
|
| 856 | _uhttp://172.23.153.220/th.pdf | ||
| 905 |
_aNazla _eRevisor |
||
| 905 |
_aSamia _eCataloger |
||
| 942 |
_2ddc _cTH |
||
| 999 |
_c41513 _d41513 |
||