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Acta Haematologica|January 1, 1976
A 2d case of haemoglobin Belfast (beta 15 (A 12) Trp replaced by Arg) observed in a French patientG Gacon, H Wajcman, D Labie, et al.Haematologia|January 1, 1986
Heterogeneity of sickle cell disease as shown by density profiles: effects of fetal hemoglobin and alpha thalassemiaV Baudin, J Pagnier, D Labie, et al.Echocardiography (Mount Kisco, N.Y.)|February 15, 2001
Imaging in Cardiac EchinococcosisAhmed Bennis, C. Bennani-Smirés, N. ChraibiHormone Research|January 1, 1997
Genetic alterations of the RET proto-oncogene in familial and sporadic pheochromocytomasP Rodien, X Jeunemaitre, C Dumont, et al.La Nouvelle Presse Medicale|January 26, 1980
[Polycythemia resulting from abnormal hemoglobin with increased affinity for oxygen. Two cases (author's transl)]G Gacon, H Wajcman, O Belkhodja-Dunda, et al.Biomedicine / [Publiee Pour L'A.A.I.C.I.G.]|June 1, 1976
A case of hemoglobin M Boston. New data about valency hybrids brought by isoelectrofocusing studyR Krishnamoorthy, H Wajcman, D Labie, et al.Nouvelle Revue Francaise D'Hematologie|January 1, 1981
Hemoglobin Barcelona beta 94 (FG1) Asp leads to His : a new hemoglobin Variant with increased oxygen affinityJ L Aguilar i Bascompte, H Wajcman, C Poyart, et al.Blood|August 1, 1983
Alpha-thalassemia is related to prolonged survival in sickle cell anemiaJ G Mears, H M Lachman, D Labie, et al.Nouvelle Revue Francaise D'Hematologie|January 1, 1979
[Hemoglobin G Coushatta (beta 22 (B4) glu leads to ala) in Algeria: an homozygous case]J P Boissel, H Wajcman, D Labie, et al.Journal of Intellectual Disability Research : JIDR|April 16, 1998
Prevalence of fragile-X syndrome and FRAXE among children with intellectual disability in a Caribbean island, Guadeloupe, French West IndiesA Elbaz, J Suédois, M Duquesnoy, et al.Pageof 20