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R B Colah

Showing results (21-30 of 36) with videos related to

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Journal of Postgraduate Medicine|March 26, 2013
Detection of fetal mutations causing hemoglobinopathies by non-invasive prenatal diagnosis from maternal plasmaE D'Souza, P M Sawant, A H Nadkarni, et al.
Genetics and Molecular Research : GMR|October 24, 2007
First-trimester prenatal diagnosis of pyruvate kinase deficiency in an Indian family with the pyruvate kinase-Amish mutationP S Kedar, S Nampoothiri, S Sreedhar, et al.
British Journal of Haematology|May 1, 1997
Beta-thalassaemia heterozygotes with alpha-globin gene triplicationR B Colah, A H Nadkarni, M B Mukherjee, et al.
American Journal of Hematology|April 3, 2001
Symptomatic presentation of a sickle cell heterozygote: an evaluation of genetic factorsM B Mukherjee, R R Surve, A C Gorakshakar, et al.
Indian Journal of Human Genetics|November 20, 2010
Microsatellite diversity among the primitive tribes of IndiaMalay B Mukherjee, V Tripathy, R B Colah, et al.
Hemoglobin|February 24, 2001
A simple approach to the characterization of three common Indian beta-thalassemia mutations by artificially created restriction sitesA R Pawar, C Y Lu, C Besmond, et al.
Indian Journal of Pediatrics|August 19, 2007
HPLC studies in hemoglobinopathiesR B Colah, R Surve, P Sawant, et al.
Hemoglobin|October 10, 1997
Prenatal diagnosis of beta-thalassemia among Indians using denaturing gradient gel electrophoresisA C Gorakshakar, C P Lulla, A H Nadkarni, et al.
American Journal of Hematology|June 15, 1999
Potential of denaturing gradient gel electrophoresis for scanning of beta-thalassemia mutations in IndiaA C Gorakshakar, A R Pawar, A H Nadkarni, et al.
Community Genetics|February 13, 2004
Genetic disorders in haematological practice in IndiaD Mohanty, R B Colah, A C Gorakshakar, et al.
Pageof 4

Showing results (21-30 of 36) with videos related to

Sort By:
Pageof 4
Journal of Postgraduate Medicine|March 26, 2013
Detection of fetal mutations causing hemoglobinopathies by non-invasive prenatal diagnosis from maternal plasmaE D'Souza, P M Sawant, A H Nadkarni, et al.
Genetics and Molecular Research : GMR|October 24, 2007
First-trimester prenatal diagnosis of pyruvate kinase deficiency in an Indian family with the pyruvate kinase-Amish mutationP S Kedar, S Nampoothiri, S Sreedhar, et al.
British Journal of Haematology|May 1, 1997
Beta-thalassaemia heterozygotes with alpha-globin gene triplicationR B Colah, A H Nadkarni, M B Mukherjee, et al.
American Journal of Hematology|April 3, 2001
Symptomatic presentation of a sickle cell heterozygote: an evaluation of genetic factorsM B Mukherjee, R R Surve, A C Gorakshakar, et al.
Indian Journal of Human Genetics|November 20, 2010
Microsatellite diversity among the primitive tribes of IndiaMalay B Mukherjee, V Tripathy, R B Colah, et al.
Hemoglobin|February 24, 2001
A simple approach to the characterization of three common Indian beta-thalassemia mutations by artificially created restriction sitesA R Pawar, C Y Lu, C Besmond, et al.
Indian Journal of Pediatrics|August 19, 2007
HPLC studies in hemoglobinopathiesR B Colah, R Surve, P Sawant, et al.
Hemoglobin|October 10, 1997
Prenatal diagnosis of beta-thalassemia among Indians using denaturing gradient gel electrophoresisA C Gorakshakar, C P Lulla, A H Nadkarni, et al.
American Journal of Hematology|June 15, 1999
Potential of denaturing gradient gel electrophoresis for scanning of beta-thalassemia mutations in IndiaA C Gorakshakar, A R Pawar, A H Nadkarni, et al.
Community Genetics|February 13, 2004
Genetic disorders in haematological practice in IndiaD Mohanty, R B Colah, A C Gorakshakar, et al.
Pageof 4