المؤلفون: Forni G.L., Caforio P., Pinto V., Pignataro P., Radhakrishnan K., Unal S., Tomaiuolo G., Iolascon A., Russo R., Andolfo I., Manna F., Gambale A., Marra R., Rosato B.E.

مصطلحات الفهرس: hereditary anemia/di [Diagnosis], Blackfan Diamond anemia/di [Diagnosis], Blackfan Diamond anemia/et [Etiology], brain disease, child, clinical feature, cohort analysis, congenital dyserythropoietic anemia/cn [Congenital Disorder], congenital dyserythropoietic anemia/di [Diagnosis], controlled study, diagnostic procedure, diagnostic value, disease association, disease severity, epilepsy, family, female, gene, gene mutation, genetic analysis, genetic disorder/cn [Congenital Disorder], genetic disorder/di [Diagnosis], genetic disorder/et [Etiology], genotype, hemolytic anemia/cn [Congenital Disorder], hemolytic anemia/di [Diagnosis], hemolytic anemia/et [Etiology], hereditary spherocytosis/cn [Congenital Disorder], hereditary spherocytosis/di [Diagnosis], hereditary spherocytosis/et [Etiology], high throughput sequencing, homozygote, human, infant, inheritance, iron overload/co [Complication], major clinical study, male, patient care, phenotype, preschool child, priority journal, school child, stomatocytosis/cn [Congenital Disorder], stomatocytosis/di [Diagnosis], stomatocytosis/et [Etiology], genomic DNA/ec [Endogenous Compound], CAD gene, hereditary anemia/cn [Congenital Disorder], hereditary anemia/et [Etiology], infantile epileptic encephalopathy, piezo1 gene, PKLR gene, SEC23B gene, adolescent, anemia/cn [Congenital Disorder], anemia/di [Diagnosis], anemia/et [Etiology], article, Blackfan Diamond anemia/cn [Congenital Disorder], Article

URL: https://repository.monashhealth.org/monashhealthjspui/handle/1/37000
American Journal of Hematology
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المؤلفون: Forni G.L., Caforio P., Pinto V., Pignataro P., Radhakrishnan K., Unal S., Tomaiuolo G., Iolascon A., Russo R., Andolfo I., Manna F., Gambale A., Marra R., Rosato B.E.

مصطلحات الفهرس: hereditary anemia/di [Diagnosis], Blackfan Diamond anemia/di [Diagnosis], Blackfan Diamond anemia/et [Etiology], brain disease, child, clinical feature, cohort analysis, congenital dyserythropoietic anemia/cn [Congenital Disorder], congenital dyserythropoietic anemia/di [Diagnosis], controlled study, diagnostic procedure, diagnostic value, disease association, disease severity, epilepsy, family, female, gene, gene mutation, genetic analysis, genetic disorder/cn [Congenital Disorder], genetic disorder/di [Diagnosis], genetic disorder/et [Etiology], genotype, hemolytic anemia/cn [Congenital Disorder], hemolytic anemia/di [Diagnosis], hemolytic anemia/et [Etiology], hereditary spherocytosis/cn [Congenital Disorder], hereditary spherocytosis/di [Diagnosis], hereditary spherocytosis/et [Etiology], high throughput sequencing, homozygote, human, infant, inheritance, iron overload/co [Complication], major clinical study, male, patient care, phenotype, preschool child, priority journal, school child, stomatocytosis/cn [Congenital Disorder], stomatocytosis/di [Diagnosis], stomatocytosis/et [Etiology], genomic DNA/ec [Endogenous Compound], CAD gene, hereditary anemia/cn [Congenital Disorder], hereditary anemia/et [Etiology], infantile epileptic encephalopathy, piezo1 gene, PKLR gene, SEC23B gene, adolescent, anemia/cn [Congenital Disorder], anemia/di [Diagnosis], anemia/et [Etiology], article, Blackfan Diamond anemia/cn [Congenital Disorder], Article

URL: https://repository.monashhealth.org/monashhealthjspui/handle/1/37000
American Journal of Hematology
Click here for full text options
LibKey Link