GENETIC SCREENING FOR SICKLE CELL DISEASE AND GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY IN NEWBORN INFANTS
Ebtesam Mohamed Abdallah;
Abstract
The present study aimed at screening newborns for two of the commonest congenital hemolytic anemias; sickle cell disease and G6PD deficiency, in order to identify the affected infants as early as possible, to offer their families the proper generic counse
Other data
| Title | GENETIC SCREENING FOR SICKLE CELL DISEASE AND GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY IN NEWBORN INFANTS | Other Titles | المسح الوراثى لمرض الخلايا المنجلية ونقص انزيم الجلولوكوز - 6 فوسفات ديهيدروجينير فى الاطفال حديثى الولادة | Authors | Ebtesam Mohamed Abdallah | Keywords | GENETIC SCREENING FOR SICKLE CELL DISEASE AND GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY IN NEWBORN INFANTS | Issue Date | 2002 | Description | The present study aimed at screening newborns for two of the commonest congenital hemolytic anemias; sickle cell disease and G6PD deficiency, in order to identify the affected infants as early as possible, to offer their families the proper generic counse |
Recommend this item
Similar Items from Core Recommender Database
Items in Ain Shams Scholar are protected by copyright, with all rights reserved, unless otherwise indicated.