Molecular pathogenesis and clinical management of Fanconi anemia

Fanconi anemia (FA) is a rare genetic disorder associated with a high frequency of hematological abnormalities and congenital anomalies. Based on multilateral efforts from basic scientists and clinicians, significant advances in our knowledge of FA have been made in recent years. Here we review the...

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Vydáno v:	The Journal of clinical investigation Ročník 122; číslo 11; s. 3799 - 3806
Hlavní autoři:	Kee, Younghoon, D’Andrea, Alan D.
Médium:	Journal Article
Jazyk:	angličtina
Vydáno:	United States American Society for Clinical Investigation 01.11.2012
Témata:	Anemia Animals Biomedical research Bone marrow Cancer Care and treatment Cell cycle Cellular proteins Chromosomes Congenital defects Congenital diseases Development and progression Diagnosis Diagnostic tests DNA repair Fanconi Anemia - diagnosis Fanconi Anemia - genetics Fanconi Anemia - metabolism Fanconi Anemia - pathology Fanconi Anemia - therapy Fanconi syndrome Fanconi's anemia Fertility Genes Genetic disorders Growth hormones Hematology Humans Insulin Mutation Pathophysiology Patients Properties Reviews Science in Medicine United States
ISSN:	0021-9738, 1558-8238, 1558-8238
On-line přístup:	Získat plný text
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