المؤلفون: Prem Kumar, M.^{Aff1, IDs4297902402941y_cor1}, Ravi Shankar, H., Deepa, K. R., Raghavendra, H. S., Shankar, Truptha

المصدر: SN Computer Science. 5(6)

المؤلفون: Shankar, N. V. S.^Aff5, Jitendra, K. V.^Aff5, Ravi Shankar, H.^Aff6, Manikumar, M.^Aff5

المساهمون: Voruganti, Hari Kumar, editor^Aff1, Kumar, K. Kiran, editor^Aff2, Krishna, P. Vamsi, editor^Aff3, Jin, Xiaoliang, editor^Aff4

المصدر: Advances in Applied Mechanical Engineering : Select Proceedings of ICAMER 2019. :433-441

المؤلفون: Shankar, N.V.S., Ravi Shankar, H., Pavan Kumar, N., Saichandu, K.

المصدر: In Materials Today: Proceedings 2020 24 Part 2:788-797

المؤلفون: RamShankar M; Molecular Biology and Genetics Unit, Jawaharlal Nehru Centre for Advanced Scientific Research, Bangalore, India., Girirajan S, Dagan O, Ravi Shankar HM, Jalvi R, Rangasayee R, Avraham KB, Anand A

المصدر: Journal of medical genetics [J Med Genet] 2003 May; Vol. 40 (5), pp. e68.

نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: British Medical Association Country of Publication: England NLM ID: 2985087R Publication Model: Print Cited Medium: Internet ISSN: 1468-6244 (Electronic) Linking ISSN: 00222593 NLM ISO Abbreviation: J Med Genet Subsets: MEDLINE

مواضيع طبية MeSH: Founder Effect*, Connexins/*genetics , Hearing Loss/*genetics , Mutation/*genetics, Amino Acid Sequence ; Audiology ; Connexin 26 ; Connexins/chemistry ; Consanguinity ; DNA Mutational Analysis ; Gene Frequency ; Genotype ; Hearing Loss/congenital ; Humans ; India ; Molecular Sequence Data ; Phenotype ; Polymorphism, Genetic/genetics