A high level of Hb F unmasks a new case of Hb Wanjiang (β (F3-F4) Ala87_Thr88delinsSer_Gln (HBB:c.255_264 delinsTTTTTCTCAG)) in a pregnant woman of African ancestry.

Autor: Pissard S; Genetics Department, APHP, GHU Henri Mondor, Créteil, France.; Medicine School, University Paris Est Creteil (UPEC) and IMRB-U955 eq2, Créteil, France., Moyrand CB; Department of Obstetrics and Gynecology, Ch Versailles André Mignot, Le Chesnay, France., Peron A; Genetics Department, APHP, GHU Henri Mondor, Créteil, France., Bodereau V; Genetics Department, APHP, GHU Henri Mondor, Créteil, France., Bichr A; Newborn Screening Department, Biochemistry-Hormonology Laboratory, Robert Debré Hospital, AP-HP, Paris, France., El Osta M; R&D Department, Biomanéo, Dijon, France., Gouriou Y; R&D Department, Biomanéo, Dijon, France., Ducoroy P; R&D Department, Biomanéo, Dijon, France., Wajcman H; Medicine School, University Paris Est Creteil (UPEC) and IMRB-U955 eq2, Créteil, France.

Publikováno v: International journal of laboratory hematology [Int J Lab Hematol] 2023 Dec; Vol. 45 (6), pp. 990-994. Date of Electronic Publication: 2023 Jul 04.

Hemoglobinopathy testing: the significance of accuracy and pitfalls in HbA2 determination.

Autor: Wajcman, H.¹ Henri.Wajcman@inserm.fr, Azimi, M.², Cui, J.², Hoppe, C.², Flamini, M.³, Ho, C.⁴, Reddy, S.⁴

Publikováno v: International Journal of Laboratory Hematology. Feb2017, Vol. 39 Issue 1, pe23-e27. 5p.

Common Haplotype Dependency of High G γ -globin Gene Expression and High Hb F Levels in β -thalassemia and Sickle Cell Anemia Patients

Autor: Labie, D., Pagnier, J., Lapoumeroulie, C., Rouabhi, F., Dunda-Belkhodja, O., Chardin, P., Beldjord, C., Wajcman, H., Fabry, M. E., Nagel, R. L.

Publikováno v: Proceedings of the National Academy of Sciences of the United States of America, 1985 Apr 01. 82(7), 2111-2114.

Externí odkaz: https://www.jstor.org/stable/25045

Hémoglobines : structure et fonction

Autor: Wajcman, H.

Publikováno v: In EMC - Hematologie 2005 2(3):145-157

Short insertion in a hemoglobin chain: Hb Esch, an unstable α1 variant with duplication of the sequence Ala 65-Leu-Thr-Asn 68

Autor: Préhu, C, Groff, P, Kalmes, G, Golinska, B, Riou, J, Prome, D, Richelme-David, S, Kiger, L, Ducrocq, R, Wajcman, H

Publikováno v: In Blood Cells, Molecules and Diseases 2003 31(2):234-239