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

By:

Hanan Mohamed Ali Ahmed

Contributor(s):

Material type: Text

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]

Subject(s):

Online resources:

Click here to access online

Available additional physical forms:

Issued also as CD

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

Tags from this library: No tags from this library for this title. Log in to add tags.

Average rating: 0.0 (0 votes)

Holdings
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

Browsing المكتبة المركزبة الجديدة - جامعة القاهرة shelves Close shelf browser (Hides shelf browser)

Previous	No cover image available	No cover image available	No cover image available	No cover image available	No cover image available	No cover image available	No cover image available	Next
Previous	Cai01.11.07.Ph.D.2009.Ge.P The prevalence of human platelet antigen(HPA)1a and 1bb group among Egyptian pregnant females and the incidence of HPA1a alloimmunization in neonates /	Cai01.11.07.Ph.D.2009.Ge.P The prevalence of human platelet antigen(HPA)1a and 1bb group among Egyptian pregnant females and the incidence of HPA1a alloimmunization in neonates /	Cai01.11.07.Ph.D.2009.Ha.M Molecular study of factor VIII gene in Egyptian patients with hemophilia A /	Cai01.11.07.Ph.D.2009.Ha.M Molecular study of factor VIII gene in Egyptian patients with hemophilia A /	Cai01.11.07.Ph.D.2009.Ha.P Paraoxonase gene polymorphism as a marker for early microvascular complications in type 1 diabetes mellitus /	Cai01.11.07.Ph.D.2009.Ha.P Paraoxonase gene polymorphism as a marker for early microvascular complications in type 1 diabetes mellitus /	Cai01.11.07.Ph.D.2009.Ha.P The prognostic significance of chromosome 11 q22.3 deletion in chronic lymphocytic leukemia /	Next

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

There are no comments on this title.

to post a comment.

Click on an image to view it in the image viewer