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P K Sukumaran

Showing results (1-10 of 18) with videos related to

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The Journal of the Association of Physicians of India|July 1, 1978
ThalassaemiasP K Sukumaran
British Journal of Haematology|July 1, 1973
A second type of hereditary persistence of foetal haemoglobin in IndiaW A Schroeder, T H Huisman, P K Sukumaran
Journal of the Indian Medical Association|July 16, 1970
Hypochromic anaemia caused by beta-thalassaemia traitB C Mehta, P K Sukumaran, J C Patel
British Journal of Haematology|August 1, 1984
Restriction endonuclease gene mapping studies of an Indian (A gamma delta beta)zero-thalassaemia, previously identified as G gamma-HPFHT Nakatsuji, J G Gilman, P K Sukumaran, et al.
Indian Pediatrics|June 1, 1973
Hemoglobin-M diseaseR T Bajaj, R M Malik, M Desai, et al.
Indian Pediatrics|February 1, 1987
Hb H diseaseB R Agarwal, R H Merchant, P K Sukumaran, et al.
Indian Journal of Pathology & Bacteriology|January 1, 1975
Haemoglobin-m disease in a punjabi hindu familyK C Das, P S Bidwai, S S Mahapatra, et al.
Indian Pediatrics|May 1, 1974
Congenital erythropoietic porphyria: a case report and review of the literatureM H Seervai, R H Merchant, S M Merchant, et al.
Journal of Medical Genetics|December 1, 1972
Haemoglobin Q India (alpha 64(E13) aspartic acid histidine) associated with beta-thalassemia observed in three Sindhi familiesP K Sukumaran, S M Merchant, M P Desai, et al.
Acta Haematologica|January 1, 1971
Hereditary eliptocytosis associates with beta-thalassaemia and a variant of Rh (D). A study in a Sinhalese familyN Nagaratnam, K A Siripala, A M Attapatu, et al.
Pageof 2

Showing results (1-10 of 18) with videos related to

Sort By:
Pageof 2
The Journal of the Association of Physicians of India|July 1, 1978
ThalassaemiasP K Sukumaran
British Journal of Haematology|July 1, 1973
A second type of hereditary persistence of foetal haemoglobin in IndiaW A Schroeder, T H Huisman, P K Sukumaran
Journal of the Indian Medical Association|July 16, 1970
Hypochromic anaemia caused by beta-thalassaemia traitB C Mehta, P K Sukumaran, J C Patel
British Journal of Haematology|August 1, 1984
Restriction endonuclease gene mapping studies of an Indian (A gamma delta beta)zero-thalassaemia, previously identified as G gamma-HPFHT Nakatsuji, J G Gilman, P K Sukumaran, et al.
Indian Pediatrics|June 1, 1973
Hemoglobin-M diseaseR T Bajaj, R M Malik, M Desai, et al.
Indian Pediatrics|February 1, 1987
Hb H diseaseB R Agarwal, R H Merchant, P K Sukumaran, et al.
Indian Journal of Pathology & Bacteriology|January 1, 1975
Haemoglobin-m disease in a punjabi hindu familyK C Das, P S Bidwai, S S Mahapatra, et al.
Indian Pediatrics|May 1, 1974
Congenital erythropoietic porphyria: a case report and review of the literatureM H Seervai, R H Merchant, S M Merchant, et al.
Journal of Medical Genetics|December 1, 1972
Haemoglobin Q India (alpha 64(E13) aspartic acid histidine) associated with beta-thalassemia observed in three Sindhi familiesP K Sukumaran, S M Merchant, M P Desai, et al.
Acta Haematologica|January 1, 1971
Hereditary eliptocytosis associates with beta-thalassaemia and a variant of Rh (D). A study in a Sinhalese familyN Nagaratnam, K A Siripala, A M Attapatu, et al.
Pageof 2