Connexin 26 gene in non-syndromic hearing loss / (Record no. 41513)
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000 -LEADER | |
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fixed length control field | 01716cam a2200349 a 4500 |
003 - CONTROL NUMBER IDENTIFIER | |
control field | EG-GiCUC |
005 - DATE AND TIME OF LATEST TRANSACTION | |
control field | 20250223030751.0 |
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION | |
fixed length control field | 130216s2012 ua d f m 000 0 eng d |
040 ## - CATALOGING SOURCE | |
Original cataloging agency | EG-GiCUC |
Language of cataloging | eng |
Transcribing agency | EG-GiCUC |
041 0# - LANGUAGE CODE | |
Language code of text/sound track or separate title | eng |
049 ## - LOCAL HOLDINGS (OCLC) | |
Holding library | Deposite |
097 ## - Thesis Degree | |
Thesis Level | Ph.D |
099 ## - LOCAL FREE-TEXT CALL NUMBER (OCLC) | |
Classification number | Cai01.11.12.Ph.D.2012.Mo.C |
100 0# - MAIN ENTRY--PERSONAL NAME | |
Personal name | Mona Ahmed Elakkad |
245 10 - TITLE STATEMENT | |
Title | Connexin 26 gene in non-syndromic hearing loss / |
Statement of responsibility, etc. | Mona Ahmed Elakkad ; Supervised Ahmad Sameh Farid , Mohamed Ibrahim Shabana , Maha Hassan AbouElew |
246 15 - VARYING FORM OF TITLE | |
Title proper/short title | ضعف السمع الغير متلازم و الجين كونكسين ٢٦ |
260 ## - PUBLICATION, DISTRIBUTION, ETC. | |
Place of publication, distribution, etc. | Cairo : |
Name of publisher, distributor, etc. | Mona Ahmed Elakkad , |
Date of publication, distribution, etc. | 2012 |
300 ## - PHYSICAL DESCRIPTION | |
Extent | 111 P. : |
Other physical details | charts ; |
Dimensions | 25cm |
502 ## - DISSERTATION NOTE | |
Dissertation note | Thesis (Ph.D.) - Cairo University - Faculty of Medicine - Department of E.N.T |
520 ## - SUMMARY, ETC. | |
Summary, etc. | Mutations 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 ## - ADDITIONAL PHYSICAL FORM AVAILABLE NOTE | |
Additional physical form available note | Issued also as CD |
653 #4 - INDEX TERM--UNCONTROLLED | |
Uncontrolled term | Connexin 26 |
653 #4 - INDEX TERM--UNCONTROLLED | |
Uncontrolled term | GJB2 |
653 #4 - INDEX TERM--UNCONTROLLED | |
Uncontrolled term | Nonsyndromic autosomal recessive sensorineural hearing loss |
700 0# - ADDED ENTRY--PERSONAL NAME | |
Personal name | Ahmad Sameh Farid , |
Relator term | |
700 0# - ADDED ENTRY--PERSONAL NAME | |
Personal name | Maha Hassan AbouElew , |
Relator term | |
700 0# - ADDED ENTRY--PERSONAL NAME | |
Personal name | Mohamed Ibrahim Shabana , |
Relator term | |
856 ## - ELECTRONIC LOCATION AND ACCESS | |
Uniform Resource Identifier | <a href="http://172.23.153.220/th.pdf">http://172.23.153.220/th.pdf</a> |
905 ## - LOCAL DATA ELEMENT E, LDE (RLIN) | |
Cataloger | Nazla |
Reviser | Revisor |
905 ## - LOCAL DATA ELEMENT E, LDE (RLIN) | |
Cataloger | Samia |
Reviser | Cataloger |
942 ## - ADDED ENTRY ELEMENTS (KOHA) | |
Source of classification or shelving scheme | Dewey Decimal Classification |
Koha item type | Thesis |
Source of classification or shelving scheme | Not for loan | Home library | Current library | Date acquired | Full call number | Barcode | Date last seen | Koha item type | Copy number |
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Dewey Decimal Classification | المكتبة المركزبة الجديدة - جامعة القاهرة | قاعة الرسائل الجامعية - الدور الاول | 11.02.2024 | Cai01.11.12.Ph.D.2012.Mo.C | 01010110059622000 | 22.09.2023 | Thesis | ||
Dewey Decimal Classification | المكتبة المركزبة الجديدة - جامعة القاهرة | مخـــزن الرســائل الجـــامعية - البدروم | 11.02.2024 | Cai01.11.12.Ph.D.2012.Mo.C | 01020110059622000 | 22.09.2023 | CD - Rom | 59622.CD |