9 results on '"Chowdhury, Madhumita Roy"'
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2. Mutation Spectrum of Tuberous Sclerosis Complex Patients in Indian Population
3. Prenatal diagnosis of steroid 21-hydroxylase-deficient congenital adrenal hyperplasia: Experience from a tertiary care centre in India
4. Mutation Spectrum of Tuberous Sclerosis Complex Patients in Indian Population
5. Application of chromosomal microarrays in the evaluation of intellectual disability/global developmental delay patients – A study from a tertiary care genetic centre in India
6. Frequency of primary mutations of Leber's hereditary optic neuropathy patients in North Indian population.
7. Factor IX gene polymorphisms in Indian population
8. Identification of a novel homozygous mutation in transmembrane channel like 1 (TMC1) gene, one of the second-tier hearing loss genes after GJB2 in India.
9. Molecular characterization of hemophilia B in North Indian families: identification of novel and recurrent molecular events in the factor IX gene.
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