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Hemoglobin|February 2, 2013
Hb Plasencia [α125(H8)Leu→Arg (α2)] is a frequent cause of α+-thalassemia in the Portuguese populationElizabete Cunha, Celeste Bento, Ana Oliveira, et al.Hemoglobin|February 27, 2013
Sistani population: a different spectrum of β-thalassemia mutations from other ethnic groups of IranEbrahim Miri-Moghaddam, Azita Zadeh-Vakili, Abbas Nikravesh, et al.Hemoglobin|March 9, 2013
Identification of the first mutation in a BRE motif of the β-globin gene and its inheritance with two other α-globin gene mutations in a Lebanese familyAdlette Inati, Hussein A Abbas, Jad Al-Danaf, et al.Hemoglobin|February 14, 2013
Novel mutations responsible for α-thalassemia in Iranian familiesNooshin Bayat, Samaneh Farashi, Nima Hafezi-Nejad, et al.Hemoglobin|February 9, 2013
Detection of Hb Constant Spring [α142, Term→Gln, TAA>CAA (α2)] in heterozygotes combined with β-thalassemiaYou-Qiong Li, Ru Li, Dong-Zhi LiHemoglobin|February 24, 2012
Association of Hb New York with Hb E and α(0)-thalassemia in a Chinese woman identified by Sebia CapillaryS2 systemDong-Zhi Li, Jian-Ying Zhou, Xing-Mei Xie, et al.Hemoglobin|March 21, 2012
First detection of Hb Taybe [α38(C3) or α39(C4) Thr→0 (α1)] in an Italian childMaria Elisabetta Paglietti, Maria Carla Sollaino, Daniela Loi, et al.Hemoglobin|November 28, 2012
A single-tube multiplex gap-polymerase chain reaction for the detection of eight β-globin gene cluster deletions common in Southeast AsiaJaruwan Tritipsombut, Marion Phylipsen, Vip Viprakasit, et al.Hemoglobin|April 23, 2013
β-Thalassemia in Abu Dhabi: consanguinity and tribal stratification are major factors explaining the high prevalence of the diseaseSrdjan Denic, Bashir Aden, Nico Nagelkerke, et al.Hemoglobin|May 16, 2013
Hb AHVAZ [α83(F4)Leu→Arg, CTG>CGG (α2); HBA2: c.251T>G],a new hemoglobin variant of the α2-globin geneMohammad Hamid, Gholamreza Shariati, Alihossein Saberi, et al.Pageof 238