Frequency of hemochromatosis (HFE ) gene mutations among B - thalassaemic patients with iron overload / (Record no. 30541)
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000 -LEADER | |
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fixed length control field | 01839cam a2200325 a 4500 |
003 - CONTROL NUMBER IDENTIFIER | |
control field | EG-GiCUC |
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION | |
fixed length control field | 100603s2010 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 | M.Sc |
099 ## - LOCAL FREE-TEXT CALL NUMBER (OCLC) | |
Classification number | Cai01.10.04.M.Sc.2010.Do.F |
100 0# - MAIN ENTRY--PERSONAL NAME | |
Personal name | Doaa Mohammed Taher Abdelmohsen |
245 10 - TITLE STATEMENT | |
Title | Frequency of hemochromatosis (HFE ) gene mutations among B - thalassaemic patients with iron overload / |
Statement of responsibility, etc. | Doaa Mohammed Taher Abdelmohsen ; Supervised Magdy Ahmed Elsayed Ghoniem , Eman Moawad Mohammed Gouda , Nermeen Ahmed Eldesoukey |
246 15 - VARYING FORM OF TITLE | |
Title proper/short title | دراسة معدل الطفرات فى جين الهيموكروماتوزس فى مرضى الثلاثيما المعرضين لزيادة عنصر الحديد |
260 ## - PUBLICATION, DISTRIBUTION, ETC. | |
Place of publication, distribution, etc. | Cairo : |
Name of publisher, distributor, etc. | Doaa Mohammed Taher Abdelmohsen , |
Date of publication, distribution, etc. | 2010 |
300 ## - PHYSICAL DESCRIPTION | |
Extent | 126Leaves : |
Other physical details | charts ; |
Dimensions | 30cm |
502 ## - DISSERTATION NOTE | |
Dissertation note | Thesis (M.Sc.) - Cairo University - Faculty of Veterinary Medicine - Department of Biochemistry and Chemistry of Nutrition |
520 ## - SUMMARY, ETC. | |
Summary, etc. | Ý- thalassemia one of the most severe form of thalassemia is caused by defective globin production that causes anemia and also it results in iron overload which is the major cause of Ý- thalassemia mortality worldwide . Hereditary hemochromatosis is a disorder of iron metabolism characterized by increased iron intake and progressive storage and is related to mutations in the HFE gene |
530 ## - ADDITIONAL PHYSICAL FORM AVAILABLE NOTE | |
Additional physical form available note | Issued also as CD |
653 #4 - INDEX TERM--UNCONTROLLED | |
Uncontrolled term | Hemochromatosis (HFE ) gene |
653 #4 - INDEX TERM--UNCONTROLLED | |
Uncontrolled term | Hereditary hemochromatosis (HH ) |
653 #4 - INDEX TERM--UNCONTROLLED | |
Uncontrolled term | Ý- thalassemia |
700 0# - ADDED ENTRY--PERSONAL NAME | |
Personal name | Eman Moawad Mohammed Gouda , |
Relator term | |
700 0# - ADDED ENTRY--PERSONAL NAME | |
Personal name | Magdy Ahmed Elsayed Ghoniem , |
Relator term | |
700 0# - ADDED ENTRY--PERSONAL NAME | |
Personal name | Nermeen Ahmed Eldesoukey , |
Relator term | |
905 ## - LOCAL DATA ELEMENT E, LDE (RLIN) | |
Cataloger | Fatma |
Reviser | Cataloger |
905 ## - LOCAL DATA ELEMENT E, LDE (RLIN) | |
Cataloger | Nazla |
Reviser | Revisor |
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 | Cai01.10.04.M.Sc.2010.Do.F | 01010110053320000 | 22.09.2023 | Thesis | ||
Dewey Decimal Classification | المكتبة المركزبة الجديدة - جامعة القاهرة | مخـــزن الرســائل الجـــامعية - البدروم | 11.02.2024 | Cai01.10.04.M.Sc.2010.Do.F | 01020110053320000 | 22.09.2023 | CD - Rom | 53320.CD |