S. Sinha

Utility of family studies in diagnosing abnormal hemoglobins/thalassemic states

I. Verma, R. Saxena, M. Bhargava, 2009, Indian journal of pediatrics.

High frequency of new mutations in North Indian Duchenne/Becker muscular dystrophy patients

B. Mittal, S. Mishra, S. Sinha, 1996, Clinical genetics.

Proportion and pattern of dystrophin gene deletions in North Indian Duchenne and Becker muscular dystrophy patients

B. Mittal, Vinita Singh, S. Pradhan, 1997, Human Genetics.

Detection of gene deletion in patients of Duchenne muscular dystrophy/Becker muscular dystrophy using polymerase chain reaction.

B. Mittal, S. Pradhan, S. Sinha, 1992, The Indian journal of medical research.

Genotype-phenotype correlation in Duchenne/Becker muscular dystrophy patients seen at Lucknow.

B. Mittal, S. Pradhan, L. Chaturvedi, 1997, The Indian journal of medical research.