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Connexin 26 gene in non-syndromic hearing loss / (Record no. 41513)

MARC details
000 -LEADER
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
Holdings
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
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