Sickle cell disease caused by heterozygosity for Hb S and novel LCR deletion: Report of two patients.
about
Enhancer alterations in cancer: a source for a cell identity crisis.Diagnosis and prevention of thalassemia.SIRT1 activates the expression of fetal hemoglobin genesDiverse hematological phenotypes of β-thalassemia carriers.Loss of Major DNase I Hypersensitive Sites in Duplicated β-globin Gene Cluster Incompletely Silences HBB Gene Expression.Hb S/β+-thalassemia due to Hb sickle and a novel deletion of DNase I hypersensitive sites HS3 and HS4 of the β locus control region.Genetic Basis and Genetic Modifiers of β-Thalassemia and Sickle Cell Disease.Heterozygosity for deletion of hypersensitive site 3 in the human locus control region has an unexpected minor effect on red cell phenotype.A novel deletion/insertion caused by a replication error in the β-globin gene locus control region.Severe fetal and neonatal hemolytic anemia due to a 198 kb deletion removing the complete β-globin gene cluster
P2860
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P2860
Sickle cell disease caused by heterozygosity for Hb S and novel LCR deletion: Report of two patients.
description
2009 nî lūn-bûn
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2009年の論文
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2009年学术文章
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2009年学术文章
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2009年学术文章
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2009年学术文章
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2009年学术文章
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name
Sickle cell disease caused by ...... etion: Report of two patients.
@en
Sickle cell disease caused by ...... etion: Report of two patients.
@nl
type
label
Sickle cell disease caused by ...... etion: Report of two patients.
@en
Sickle cell disease caused by ...... etion: Report of two patients.
@nl
prefLabel
Sickle cell disease caused by ...... etion: Report of two patients.
@en
Sickle cell disease caused by ...... etion: Report of two patients.
@nl
P2093
P356
P1476
Sickle cell disease caused by ...... etion: Report of two patients.
@en
P2093
David H K Chui
Esmira Becirevic
Hong-Yuan Luo
Jane S Hankins
Jason C C So
Lillian McMahon
Michael Y Li
Miriam S C Hellberg
Russell E Ware
Sara C Koenig
P304
P356
10.1002/AJH.21480
P577
2009-09-01T00:00:00Z