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Hemoglobin|January 1, 1987
Further characterization of Hb Henri Mondor or alpha 2 beta 2(26)(B8)Glu----ValJ Bardakdjian, N Arous, J Kister, et al.
Blood Cells, Molecules & Diseases|September 16, 2003
Short insertion in a hemoglobin chain: Hb Esch, an unstable alpha1 variant with duplication of the sequence Ala65-Leu-Thr-Asn68C Préhu, P Groff, G Kalmes, et al.
Human Genetics|January 1, 1981
Genetic regulation of gamma gene expression: study of the interaction of beta-thalassemia with heterocellular HPFHA M Soummer, U Testa, P Dujardin, et al.
Hemoglobin|April 13, 2001
Hb Mont Saint Aignan [beta128(H6)Ala-->Pro]: a new unstable variant leading to chronic microcytic anemiaH Wajcman, A Lahary, D Promé, et al.
Hematology and Cell Therapy|June 1, 1997
Structural and functional studies of hemoglobin Moabit (alpha 86(F7) Leu-->ArgB Gulbis, L Tshilolo, H Wajcman, et al.
European Journal of Biochemistry|December 16, 1985
Structural and functional studies of hemoglobin Poissy alpha 2 beta 2(56) (D7) Gly----Arg and 86 (F2) Ala----ProC Lacombe, C T Craescu, Y Blouquit, et al.
American Journal of Hematology|September 1, 1993
Hb Saint Nazaire (beta 103[G5]Phe-->Ile): a new example of polycythemia due to a hemoglobin variant with increased oxygen affinityH Wajcman, J Kister, A M'Rad, et al.
American Journal of Hematology|October 1, 1990
Hemoglobin Dhonburi alpha 2 beta 2 126 (H4) Val----Gly: a new unstable beta variant producing a beta-thalassemia intermedia phenotype in association with beta zero-thalassemiaJ Bardakdjian-Michau, S Fucharoen, J Delanoe-Garin, et al.
Hemoglobin|March 19, 1999
The association of Hb Khartoum [beta124(H2)Pro-->Arg] with gamma+-thalassemia is responsible for hemolytic disease in the newborn of a Sudanese familyR A Bayoumi, A Dawodu, M M Qureshi, et al.
British Journal of Haematology|March 6, 1998
Haemoglobin J-Biskra: a new mildly unstable alpha1 gene variant with a deletion of eight residues (alpha50-57, alpha51-58 or alpha52-59) including the distal histidineH Wajcman, M Dahmane, C Préhu, et al.
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