Clinical spectrum and molecular basis of recessive congenital methemoglobinemia in India von Warang, P.P., Kedar, P.S., Shanmukaiah, C., Ghosh, K., Colah, R.B.

Volltext

A successful twin pregnancy in a patient with HbE-β-thalassemia in western India von Merchant, R, Italia, K, Ahmed, J, Ghosh, K, Colah, RB

Volltext

Experience with eosin-5′-maleimide as a diagnostic tool for red cell membrane cytoskeleton disorders von Kedar, P. S., Colah, R. B., Kulkarni, S., Ghosh, K., Mohanty, D.

Volltext

Prevalence of β-thalassemia and other haemoglobinopathies in six cities in India: a multicentre study von Mohanty, D., Colah, R. B., Gorakshakar, A. C., Patel, R. Z., Master, D. C., Mahanta, J., Sharma, S. K., Chaudhari, U., Ghosh, M., Das, S., Britt, R. P., Singh, S., Ross, C., Jagannathan, L., Kaul, R., Shukla, D. K., Muthuswamy, V.

Volltext

Detection of fetal mutations causing hemoglobinopathies by non-invasive prenatal diagnosis from maternal plasma von D′Souza, E, Sawant, P, Nadkarni, A, Gorakshakar, A, Ghosh, K, Colah, R

Volltext

A novel R198H mutation in the glucose-6-phosphate dehydrogenase gene in the tribal groups of the Nilgiris in Southern India von Chalvam, R, Kedar, P S, Colah, R B, Ghosh, K, Mukherjee, M B

Volltext

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

Volltext

Microsatellite diversity among the primitive tribes of India von Mukherjee, Malay B, Tripathy, V, Colah, R B, Solanki, P K, Ghosh, K, Reddy, B M, Mohanty, D

Volltext

Molecular characterization of G6PD Insuli—a novel 989 CGC → CAC (330 Arg → His) mutation in the Indian population von Sukumar, S, Mukherjee, M.B, Colah, R.B, Mohanty, D

Volltext

Usefulness of prenatal detection of RhD typing by molecular analysis in Indians von Kulkarni, S S, Gorakshakar, A C, Colah, R B, Gupte, S C, Mohanty, D

Volltext

G6PD deficiency and malaria in India von Mohanty, D., Sukumar, S., Mukherjee, M.B., Colah, R.B.

Volltext

G6PD Namoru (208 T→ C) is the major polymorphic variant in the tribal populations in southern India von Chalvam, R., Mukherjee, M. B., Colah, R. B., Mohanty, D., Ghosh, K.

Volltext

Effect of α‐thalassemia on sickle‐cell anemia linked to the Arab‐Indian haplotype in India von Mukherjee, Malay B., Lu, Chang Yong, Ducrocq, Rolande, Gangakhedkar, Raman R., Colah, Roshan B., Kadam, Megha D., Mohanty, Dipika, Nagel, Ronald L., Krishnamoorthy, Rajagopal

Volltext

Evaluation of a capillary blood collection system for screening for hemoglobinopathies in remote areas von COLAH, R. B., WADIA, M., D'SOUZA, E., SAWANT, P. M., MOHANTY, D., MEHRA, M.

Volltext

Potential of denaturing gradient gel electrophoresis for scanning of β‐thalassemia mutations in India von Gorakshakar, A.C., Pawar, A.R., Nadkarni, A.H., Lu, C.Y., Mohanty, D., Krishnamoorthy, R., Besmond, C., Colah, R.B.

Volltext

Milder clinical course of sickle cell disease in patients with alpha thalassemia in the Indian subcontinent von Mukherjee, M B, Colah, R B, Ghosh, K, Mohanty, D, Krishnamoorthy, R

Volltext

Clinical Diversity of Sickle Cell Disease in Western India – Influence of Genetic Factors von Mukherjee, M.B., Surve, R.R., Ghosh, K., Colah, R.B., Mohanty, D.

Volltext

Alpha Genotyping in a Heterogeneous Indian Population von Nadkarni, Anita H., Gorakshakar, Ajit C., Mohanty, Dipika, Colah, Roshan B.

Volltext

Prevalence of clinically relevant (TA)n UGT1A1 promoter alleles in Indian neonates von D'Silva, Selma, Colah, Roshan B., Ghosh, Kanjaksha, Mukherjee, Malay B.

Volltext

Case Reports- Hemoglobin sickle D Punjab-a case report von Mukherjee MB, Surve RR, Gangakhedkar RR, Mohanty D, Colah RB

Volltext