HPLC studies in hemoglobinopathies von Colah, R B, Surve, R, Sawant, P, D'Souza, E, Italia, K, Phanasgaonkar, S, Nadkarni, A H, Gorakshakar, A C

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Hb Showa Yakushiji [β 110 (G12) Leu → Pro] in 3 families from Western India: First report on homozygous Hb Showa Yakushiji von Colah, R., Nadkarni, A., Gorakshakar, A., Phanasgaonkar, S., Sawant, P., Surve, R., Mohanty, D., Ghosh, K.

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Hb Q(India) and its interaction with beta-thalassaemia: a study of 64 cases from India von Phanasgaonkar, S, Colah, R, Ghosh, K, Mohanty, D, Gupte, S

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Hb Q India and its interaction with β-thalassaemia: a study of 64 cases from India von Phanasgaonkar, S, Colah, R, Ghosh, K, Mohanty, D, Gupte, S

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Three novel polymorphisms in the β globin gene von Nadkarni, A., Sakaguchi, T., Gorakshakar, A., Phanasgaonkar, S., Colah, R., Mohanty, D., Kiyama, R.

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Detection of two rare β -thalassemia mutations [-90 (C ® T) and CD 26 (C ®T)] among Indians von Colah, R, Mohanty, D, Gorakshakar, A, Phanasgaonkar, S

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An interplay of alleviating mutations in the clinical phenotype of β-thalassaemia intermedia von NADKARNI, A., SAKAGUCHI, T., GORAKSHAKAR, A., PHANASGAONKAR, S., KIYAMA, R., COLAH, R., MOHANTY, D.

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Genetic Disorders in Haematological Practice in India von Mohanty, D., Colah, R.B., Gorakshakar, A.C., Nadkarni, A.H., Phanasgaonkar, S.P., Shetty, S., Ghosh, K., Mukherjee, M.B.

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Red Cell Genetic Abnormalities, β-Globin Gene Haplotypes, and APOB Polymorphism in the Great Andamanese, A Primitive Negrito Tribe of Andaman and Nicobar Islands, India von MURHEKAR, K.M., MURHEKAR, M.V., MUKHERJEE, M.B., GORAKSHAKAR, A.C., SURVE, R., WADIA, M., PHANASGAONKAR, S., SHRIDEVI, S., ROSHAN, B. COLAH, MOHANTY, D.

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Prenatal diagnosis of sickle syndromes in India: dilemmas in counselling von Colah, Roshan, Surve, Reema, Nadkarni, Anita, Gorakshakar, Ajit, Phanasgaonkar, Supriya, Satoskar, Poornima, Mohanty, Dipika

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Hb Q^sup India^ and its interaction with [beta]-thalassaemia: a study of 64 cases from India von Phanasgaonkar, S, Colah, R, Ghosh, K, Mohanty, D, Gupte, S

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Impact of β globin gene mutations on the clinical phenotype of β thalassemia in India von Colah, Roshan, Nadkarni, Anita, Gorakshakar, Ajit, Phanasgaonkar, Supriya, Surve, Reema, Subramaniam, P.G., Bondge, Nagnath, Pujari, Kamala, Ghosh, Kanjaksha, Mohanty, Dipika

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Hb QIndia and its interaction with β-thalassaemia: a study of 64 cases from India von Phanasgaonkar, S., Colah, R., Ghosh, K., Mohanty, D., Gupte, S.

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Detection of two rare β -thalassemia mutations [-90 (C → T) and CD 26 (C →T)] among Indians von Gorakshakar A, Phanasgaonkar S, Colah R, Mohanty D

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HPLC Studies in Hemoglobinopathies : Newer Diagnostic Tests von COLAH, R. B, SURVE, R, SAWANT, P, D'SOUZA, E, ITALIA, K, PHANASGAONKAR, S, NADKARNI, A. H, GORAKSHAKAR, A. C

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Detection of two rare ? -thalassemia mutations [-90 ] among Indians von Gorakshakar, A, Phanasgaonkar, S, Colah, R, Mohanty, D

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Co-existence of the Codon 16 (-C) (β0) and Codon 10 (C→A) (β+) Mutations on the Same β-Globin Gene von Colah, Roshan B., Nadkarni, Anita, Pawar, Aruna, Gorakshakar, Ajit, Phanasgaonkar, Supriya, Mohanty, Dipika

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Hb D-AGRI [β9(A6)Ser Tyr;β121(GH4)Glu Gln]: A NEW INDIAN HEMOGLOBIN VARIANT WITH TWO AMINO ACID SUBSTITUTIONS IN THE SAME β CHAIN von Colah, Roshan, Wadia, Maharukh, Surve, Reema, Nadkarni, Anita, Phanasgaonkar, Supriya, Gorakshakar, Ajit, Mohanty, Dipika, Promé, Danielle, Wajcman, Henri

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Red Cell Genetic Abnormalities, [Beta]-Globin Gene Haplotypes, and APOB Polymorphisms in the Great Andamanese, A Primitive Negrito Tribe of Andaman and Nicobar Islands, India von Murhekar, K. M, Murhekar, M. V, Mukherjee, M. B, Gorakshakar, A. C, Surve, R, Wadia, M, Phanasgaonkar, S, Shridevi, S, Colah, Roshan B, Mohanty, D

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Detection of Rare β-Thalassemia Mutations by Denaturing Gradient Gel Electrophoresis Among Indians von Gorakshakar, Ajit C., Phanasgaonkar, Supriya P., Nadkarni, Anita H., Colah, Roshan B., Mohanty, Dipika

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