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Pediatric Blood & Cancer|February 2, 2012
Severe fetal and neonatal hemolytic anemia due to a 198 kb deletion removing the complete β-globin gene clusterMadeleine Verhovsek, Nirmish R Shah, Ibifiri Wilcox, et al.
Hemoglobin|September 22, 2010
New and known β-thalassemia determinants masked by known and new δ gene defects [Hb A(2)-Ramallah or δ6(A3)Glu→Gln, GAG>>CAG]Marion Phylipsen, Cornelis L Harteveld, Menno de Metz, et al.
The American Journal of Pathology|September 6, 2002
Deletion of decay-accelerating factor (CD55) exacerbates autoimmune disease development in MRL/lpr miceTakashi Miwa, Michael A Maldonado, Lin Zhou, et al.
Prenatal Diagnosis|February 16, 2005
Simple non-invasive prenatal detection of Hb Bart's disease by analysis of fetal erythrocytes in maternal bloodElizabeth T Lau, Yvonne K Kwok, Hong Yuan Luo, et al.
Stem Cells (Dayton, Ohio)|January 18, 2006
Identification and characterization of hemoangiogenic progenitors during cynomolgus monkey embryonic stem cell differentiationKatsutsugu Umeda, Toshio Heike, Momoko Yoshimoto, et al.
Blood Cells, Molecules & Diseases|December 12, 2017
A long noncoding RNA from the HBS1L-MYB intergenic region on chr6q23 regulates human fetal hemoglobin expressionTasha A Morrison, Ibifiri Wilcox, Hong-Yuan Luo, et al.
Hemoglobin|March 6, 2012
Compound heterozygosity for Hb S [β6(A3)Glu→Val] and Hb Kenya (Aγ81Leu-β86Ala) in a Ugandan womanZeqiu J Han, Cristina Lapuz, Jill F Rovenger, et al.
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