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Journal Articles

Variation of fetal hemoglobin and F-cell number with the LCR-HS2 polymorphism in nonanemic individuals [letter]

T Merghoub, M Maier-Redelsperger, D Labie, B Perichon, N Feingold, SP Dibenedetto, G Schiliro, P Samperi, r Ducrocq, J Elion, R Krishnamoorthy

Blood (1996) 87 (6): 2607.

https://doi.org/10.1182/blood.V87.6.2607.bloodjournal8762607

Published: 1996

Journal Articles

Perfusion chromatography allows an order of magnitude faster measurement of the G gamma: A gamma ratio in patients with an increased level of fetal hemoglobin [letter]

H Wajcman, F Galacteros, R Ducrocq

Blood (1996) 87 (4): 1655.

https://doi.org/10.1182/blood.V87.4.1655.bloodjournal8741655

Published: 1996

Journal Articles

Bicentric origin of sickle hemoglobin among the inhabitants of Mauritius Island [letter]

N Kotea, S Baligadoo, S Surran, R Ramasawmy, CY Lu, R Ducrocq, D Labie, R Krishnamoorthy, R Nagel

Blood (1995) 86 (1): 407–408.

https://doi.org/10.1182/blood.V86.1.407.bloodjournal861407

Published: 1995

Journal Articles

Variation in fetal hemoglobin parameters and predicted hemoglobin S polymerization in sickle cell children in the first two years of life: Parisian Prospective Study on Sickle Cell Disease

M Maier-Redelsperger, CT Noguchi, M de Montalembert, GP Rodgers, AN Schechter, A Gourbil, D Blanchard, JP Jais, R Ducrocq, JY Peltier

Blood (1994) 84 (9): 3182–3188.

https://doi.org/10.1182/blood.V84.9.3182.3182

Published: 1994

Journal Articles

Beta-globin gene cluster haplotype and alpha-thalassemia do not correlate with the acute clinical manifestations of sickle cell disease in children [letter]

M de Montalembert, M Maier-Redelsperger, R Girot, M Belloy, E Vilmer, R Ducrocq, C Guidal, J Elion

Blood (1993) 82 (8): 2595–2596.

https://doi.org/10.1182/blood.V82.8.2595b.2595b

Published: 1993

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Variation of fetal hemoglobin and F-cell number with the LCR-HS2 polymorphism in nonanemic individuals [letter]

Perfusion chromatography allows an order of magnitude faster measurement of the G gamma: A gamma ratio in patients with an increased level of fetal hemoglobin [letter]

Bicentric origin of sickle hemoglobin among the inhabitants of Mauritius Island [letter]

Variation in fetal hemoglobin parameters and predicted hemoglobin S polymerization in sickle cell children in the first two years of life: Parisian Prospective Study on Sickle Cell Disease

Beta-globin gene cluster haplotype and alpha-thalassemia do not correlate with the acute clinical manifestations of sickle cell disease in children [letter]

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ASH Publications

American Society of Hematology

Variation of fetal hemoglobin and F-cell number with the LCR-HS2 polymorphism in nonanemic individuals [letter]

Perfusion chromatography allows an order of magnitude faster measurement of the G gamma: A gamma ratio in patients with an increased level of fetal hemoglobin [letter]

Bicentric origin of sickle hemoglobin among the inhabitants of Mauritius Island [letter]

Variation in fetal hemoglobin parameters and predicted hemoglobin S polymerization in sickle cell children in the first two years of life: Parisian Prospective Study on Sickle Cell Disease

Beta-globin gene cluster haplotype and alpha-thalassemia do not correlate with the acute clinical manifestations of sickle cell disease in children [letter]

Email alerts

ASH Publications

American Society of Hematology

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