Molecular detection of intron 22 inversionof factor VIII gens in Egyptian hemophilia a patients / Shahira Kamal Anis ; Supervised Naela AbdElfatah Omran , Azza Mostafa Ibrahim , Hoda Mohamed AbdElghani

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Shahira Kamal Anis

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Language: Eng Publication details: Cairo : Shahira Kamal Anis , 2007Description: 136P. : charts ; 25cmOther title:

الكشف الجزيئى للانعكاس فى انترون 22 فى الجين الخاص بعامل التجلط 8 فى حالات الهيموفيليا ايه [Added title page title]

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Dissertation note: Thesis (Ph.D.) - Cairo University - Faculty Of Medicine - Department Of Clinical and Chemical Pathology Summary: Hemophilia A is a common disorder of blood coagulation caused by deficiency of factor VIII.The disorder is inheroted as an X linked recessive trait.Abnormalities in factor VIII gene include deletions , insertions , point mutations and inversion

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Item type	Current library	Home library	Call number	Copy number	Status	Barcode
Thesis	قاعة الرسائل الجامعية - الدور الاول	المكتبة المركزبة الجديدة - جامعة القاهرة	Cai01.11.07.Ph.D.2007.Sh.M (Browse shelf(Opens below))		Not for loan	01010110048205000
CD - Rom	مخـــزن الرســائل الجـــامعية - البدروم	المكتبة المركزبة الجديدة - جامعة القاهرة	Cai01.11.07.Ph.D.2007.Sh.M (Browse shelf(Opens below))	48205.CD	Not for loan	01020110048205000

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Thesis (Ph.D.) - Cairo University - Faculty Of Medicine - Department Of Clinical and Chemical Pathology

Hemophilia A is a common disorder of blood coagulation caused by deficiency of factor VIII.The disorder is inheroted as an X linked recessive trait.Abnormalities in factor VIII gene include deletions , insertions , point mutations and inversion

Issued also as CD

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