الكشف الجزيئى للانعكاس فى إنترون 22 فى الجين الخاص بعامل التجلط 8 فى حالات الهيموفيليا إيه
شهيرة كمال انيس;
Abstract
Hemophilia A is an X-linked recessively inherited bleeding
disorder characterized by deficiency of procoagulant factor VIII with
an incidence of 1/5 000-10 000 male births. Except for the common
inversion mutation in intron 22 of factor VIII gene, most ot
disorder characterized by deficiency of procoagulant factor VIII with
an incidence of 1/5 000-10 000 male births. Except for the common
inversion mutation in intron 22 of factor VIII gene, most ot
Other data
| Title | الكشف الجزيئى للانعكاس فى إنترون 22 فى الجين الخاص بعامل التجلط 8 فى حالات الهيموفيليا إيه | Authors | شهيرة كمال انيس | Keywords | الكشف الجزيئى للانعكاس فى إنترون 22 فى الجين الخاص بعامل التجلط 8 فى حالات الهيموفيليا إيه | Issue Date | 2007 | Description | Hemophilia A is an X-linked recessively inherited bleeding disorder characterized by deficiency of procoagulant factor VIII with an incidence of 1/5 000-10 000 male births. Except for the common inversion mutation in intron 22 of factor VIII gene, most ot |
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