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H Kronenberg

Showing results (121-130 of 183) with videos related to

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Hemoglobin|January 1, 1986
Hemoglobin Woodville: alpha (2)6(A4) aspartic acid----tyrosineP F Como, S Barber, R E Sage, et al.
Scandinavian Journal of Haematology|March 1, 1986
Molecular defects in 2 examples of severe Hb H diseaseR J Trent, T Wilkinson, J Yakas, et al.
British Journal of Haematology|February 13, 2001
Missense C168T in the Wiskott--Aldrich Syndrome protein gene is a common mutation in X-linked thrombocytopeniaL L Ho, J Ayling, I Prosser, et al.
Pathology|January 1, 1984
Diagnosis of alpha thalassemia in the newborn. Cord blood survey utilizing gene mappingR J Trent, P E Brock, J Yakas, et al.
British Journal of Rheumatology|April 1, 1989
Human cardiolipin as the antigen in an ELISA to detect anticardiolipin antibodiesR D Brown, J Gibson, J Wells, et al.
Annals of the Rheumatic Diseases|November 1, 1988
Ischaemic necrosis of the ilium complicating haemolytic anaemia due to an unstable haemoglobinN W McGill, P Warburton, H Kronenberg, et al.
Pathology|April 1, 1990
Red cell folate assays: some answers to current problems with radioassay variabilityR D Brown, R Jun, W Hughes, et al.
Pathology|January 1, 1986
(delta beta) zero thalassemia of the Southern Italian type. Its geographical origin and interaction with the sickle cell geneR J Trent, L Svirklys, M G Harris, et al.
Pathology|January 1, 1977
A new hybrid haemoglobin: haemoglobin Strumica/Beograd occurring in an individual with four haemoglobinsT Wilkinson, R W Carrell, S Brennan, et al.
The Australian & New Zealand Journal of Obstetrics & Gynaecology|February 1, 1982
Chronic consumptive coagulopathy with a uterine leiomyomaM G Harris, P Bannatyne, P Russell, et al.
Pageof 19

Showing results (121-130 of 183) with videos related to

Sort By:
Pageof 19
Hemoglobin|January 1, 1986
Hemoglobin Woodville: alpha (2)6(A4) aspartic acid----tyrosineP F Como, S Barber, R E Sage, et al.
Scandinavian Journal of Haematology|March 1, 1986
Molecular defects in 2 examples of severe Hb H diseaseR J Trent, T Wilkinson, J Yakas, et al.
British Journal of Haematology|February 13, 2001
Missense C168T in the Wiskott--Aldrich Syndrome protein gene is a common mutation in X-linked thrombocytopeniaL L Ho, J Ayling, I Prosser, et al.
Pathology|January 1, 1984
Diagnosis of alpha thalassemia in the newborn. Cord blood survey utilizing gene mappingR J Trent, P E Brock, J Yakas, et al.
British Journal of Rheumatology|April 1, 1989
Human cardiolipin as the antigen in an ELISA to detect anticardiolipin antibodiesR D Brown, J Gibson, J Wells, et al.
Annals of the Rheumatic Diseases|November 1, 1988
Ischaemic necrosis of the ilium complicating haemolytic anaemia due to an unstable haemoglobinN W McGill, P Warburton, H Kronenberg, et al.
Pathology|April 1, 1990
Red cell folate assays: some answers to current problems with radioassay variabilityR D Brown, R Jun, W Hughes, et al.
Pathology|January 1, 1986
(delta beta) zero thalassemia of the Southern Italian type. Its geographical origin and interaction with the sickle cell geneR J Trent, L Svirklys, M G Harris, et al.
Pathology|January 1, 1977
A new hybrid haemoglobin: haemoglobin Strumica/Beograd occurring in an individual with four haemoglobinsT Wilkinson, R W Carrell, S Brennan, et al.
The Australian & New Zealand Journal of Obstetrics & Gynaecology|February 1, 1982
Chronic consumptive coagulopathy with a uterine leiomyomaM G Harris, P Bannatyne, P Russell, et al.
Pageof 19