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Indian Journal of Human Genetics|September 11, 2013
Association between PRO12ALA polymorphism of the PPAR-γ2 gene and type 2 diabetes mellitus in Iranian patientsAzadeh Motavallian, Sasan Andalib, Golnaz Vaseghi, et al.Indian Journal of Human Genetics|September 11, 2013
Derivative chromosome 11 in a child resulting from a complex rearrangement involving chromosomes 3, 6 and 11 in father: Significance of parental karyotypingPrabhat Ranjan, Kundanbala Desai, Shailaja Gada SaxenaIndian Journal of Human Genetics|August 1, 2013
Rapid detection of chromosome X, Y, 13, 18, and 21 aneuploidies by primed in situ labeling/synthesis techniqueAshutosh Halder, Manish Jain, Isha ChaudharyIndian Journal of Human Genetics|August 1, 2013
Rapid-prenatal diagnosis through fluorescence in situ hybridization for preventing aneuploidy related birth defectsAshish Fauzdar, Mohit Chowdhry, R N Makroo, et al.Indian Journal of Human Genetics|August 1, 2013
In silico experiment with an-antigen-toll like receptor-5 agonist fusion construct for immunogenic application to Helicobacter pyloriMohamad Ali Haghighi, Ashraf Mohabati Mobarez, Ali Hatef Salmanian, et al.Indian Journal of Human Genetics|August 1, 2013
Polymerase chain reaction optimization for amplification of Guanine-Cytosine rich templates using buccal cell DNAC H W M R Chandrasekara Bhagya, W S Wijesundera Sulochana, N Perera HemamaliIndian Journal of Human Genetics|August 1, 2013
Fanconi-Bickel syndrome versus osteogenesis imperfeeta: An Iranian case with a novel mutation in glucose transporter 2 gene, and review of literatureFatemeh Hadipour, Peymaneh Sarkheil, Mehrdad Noruzinia, et al.Indian Journal of Human Genetics|August 1, 2013
Malignant infantile osteopetrosisKalenahalli Jagadish Kumar, Kasi Bandaru, Sathya Narayana Prashanth, et al.Indian Journal of Human Genetics|August 1, 2013
MICrocephaly, disproportionate pontine and cerebellar hypoplasia syndrome: A clinico-radiologic phenotype linked to calcium/calmodulin-dependent serine protein kinase gene mutationRashid Saleem, Gururaj Setty, Nahin HussainIndian Journal of Human Genetics|August 1, 2013
Triple X Egyptian woman and a Down's syndrome offspringFaeza Abdel Mogib El-DahtoryPageof 35