Molecular study of factor VIII gene in Egyptian patients with hemophilia A / Hanan Mohammed Ali Ahmed ; Supervised Hanaa Hamed Arnaout , Hanan Nour Raslan , Heba Mohammed Hassan Abouelew

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Hanan Mohamed Ali Ahmed

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TextLanguage: English Publication details: Cairo : Hanan Mohamed Ali Ahmed , 2009Description: 197 P. : charts , facsimiles ; 25cmOther title:

دراسة جزيئية لجين العامل الثامن فى المرضى المصريين المصابين بمرض هيموفيليا ا [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 an X-linked hereditary bleeding disorder caused by deficient or defective coagulation factor VIII multiple molecular defects may affect factor VIII gene such as point mutations premature stop codons deletions insertions and inversions

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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.2009.Ha.M (Browse shelf(Opens below))		Not for loan	01010110051322000
CD - Rom	مخـــزن الرســائل الجـــامعية - البدروم	المكتبة المركزبة الجديدة - جامعة القاهرة	Cai01.11.07.Ph.D.2009.Ha.M (Browse shelf(Opens below))	51322.CD	Not for loan	01020110051322000

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

Hemophilia A is an X-linked hereditary bleeding disorder caused by deficient or defective coagulation factor VIII multiple molecular defects may affect factor VIII gene such as point mutations premature stop codons deletions insertions and inversions

Issued also as CD

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