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Acta Haematologica
|
September 24, 2010
A new sickling variant 'Hb S-Wake β[(Glu6Val-Asn139 Ser)]' found in a compound heterozygote with Hb S β(Glu6Val) coinherited with homozygous α-thalassemia-2: phenotype and molecular characteristics
Ferdane Kutlar, R Redding-Lallinger, S E Meiler, et al.
Laboratory Hematology : Official Publication of the International Society for Laboratory Hematology
|
September 18, 2009
Compound heterozygosity for hemoglobin S [beta6(A3)Glu6Val] and hemoglobin Korle-Bu [beta73(E17)Asp73Asn]
Pascale S Akl, Ferdane Kutlar, Niren Patel, et al.
Hemoglobin
|
December 10, 2008
Two new hemoglobin variants: Hb Sinai-Greenspring [beta34(B16)Val-->Ile, GTC > ATC] and Hb Sinai-Bel Air [beta53(D4)Ala-->Asp, GCT > GAT]
Erin Dainer, Robert E Wenk, Ruth Luddy, et al.
Journal of Pediatric Hematology/Oncology
|
November 20, 2015
Hemoglobin F Only Syndrome at Birth: A Case of Maternal HbA2' Complicating the Diagnosis of β-Thalassemia
Marianne E M Yee, Maa-Ohui Quarmyne, Catherine Segbefia, et al.
European Journal of Haematology
|
May 23, 2009
Acute splenic complications and implications of splenectomy in hemoglobin SC disease
Karthi Subbannan, Celalettin Ustun, Kavita Natarajan, et al.
Hemoglobin
|
January 30, 2014
Two new hemoglobin variants: Hb Tallahassee [α3(A1)Ser→Tyr; HBA2: c.11C>A] and Hb madison-NC [β119(GH2)Gly→Ser; HBB: c.358G>A]
Ferdane Kutlar, Yoram Unguru, Natalia Dixon, et al.
Hemoglobin
|
January 22, 2005
A novel approach to rapid determination of betaS-globin haplotypes: sequencing of the Agamma-IVS-II region
Amy E Vinson, Aisha Walker, Dedrey Elam, et al.
Hemoglobin
|
October 2, 2014
Two new γ chain variants: Hb F-Augusta GA [(G)γ59(E3)Lys → Arg; HBG2: c.179A > G] and Hb F-Port Royal-II [(A)γ125(H3)Glu → Ala; HBG1: c.377A > C]
Ferdane Kutlar, Afshin Ameri, Niren H Patel, et al.
Journal of Pediatric Hematology/Oncology
|
November 2, 2011
Thalassemia-like phenotype in a novel complex hemoglobinopathy with α, β, δ globin chain abnormalities
Hernan Sabio, Natalia Dixon, Niren Patel, et al.
BMC Medical Genetics
|
July 23, 2003
Genetic risk factors for cerebrovascular disease in children with sickle cell disease: design of a case-control association study and genomewide screen
Gaye T Adams, Harold Snieder, Virgil C McKie, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 26) with videos related to
Sort By:
Page
of 3
Acta Haematologica
|
September 24, 2010
A new sickling variant 'Hb S-Wake β[(Glu6Val-Asn139 Ser)]' found in a compound heterozygote with Hb S β(Glu6Val) coinherited with homozygous α-thalassemia-2: phenotype and molecular characteristics
Ferdane Kutlar, R Redding-Lallinger, S E Meiler, et al.
Laboratory Hematology : Official Publication of the International Society for Laboratory Hematology
|
September 18, 2009
Compound heterozygosity for hemoglobin S [beta6(A3)Glu6Val] and hemoglobin Korle-Bu [beta73(E17)Asp73Asn]
Pascale S Akl, Ferdane Kutlar, Niren Patel, et al.
Hemoglobin
|
December 10, 2008
Two new hemoglobin variants: Hb Sinai-Greenspring [beta34(B16)Val-->Ile, GTC > ATC] and Hb Sinai-Bel Air [beta53(D4)Ala-->Asp, GCT > GAT]
Erin Dainer, Robert E Wenk, Ruth Luddy, et al.
Journal of Pediatric Hematology/Oncology
|
November 20, 2015
Hemoglobin F Only Syndrome at Birth: A Case of Maternal HbA2' Complicating the Diagnosis of β-Thalassemia
Marianne E M Yee, Maa-Ohui Quarmyne, Catherine Segbefia, et al.
European Journal of Haematology
|
May 23, 2009
Acute splenic complications and implications of splenectomy in hemoglobin SC disease
Karthi Subbannan, Celalettin Ustun, Kavita Natarajan, et al.
Hemoglobin
|
January 30, 2014
Two new hemoglobin variants: Hb Tallahassee [α3(A1)Ser→Tyr; HBA2: c.11C>A] and Hb madison-NC [β119(GH2)Gly→Ser; HBB: c.358G>A]
Ferdane Kutlar, Yoram Unguru, Natalia Dixon, et al.
Hemoglobin
|
January 22, 2005
A novel approach to rapid determination of betaS-globin haplotypes: sequencing of the Agamma-IVS-II region
Amy E Vinson, Aisha Walker, Dedrey Elam, et al.
Hemoglobin
|
October 2, 2014
Two new γ chain variants: Hb F-Augusta GA [(G)γ59(E3)Lys → Arg; HBG2: c.179A > G] and Hb F-Port Royal-II [(A)γ125(H3)Glu → Ala; HBG1: c.377A > C]
Ferdane Kutlar, Afshin Ameri, Niren H Patel, et al.
Journal of Pediatric Hematology/Oncology
|
November 2, 2011
Thalassemia-like phenotype in a novel complex hemoglobinopathy with α, β, δ globin chain abnormalities
Hernan Sabio, Natalia Dixon, Niren Patel, et al.
BMC Medical Genetics
|
July 23, 2003
Genetic risk factors for cerebrovascular disease in children with sickle cell disease: design of a case-control association study and genomewide screen
Gaye T Adams, Harold Snieder, Virgil C McKie, et al.
Page
of 3