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1دورية أكاديمية
المؤلفون: Snigdha Majumder, Rakshit Shah, Jisha Elias, Yogesh Mistry, Karunakaran Coral, Priyanka Shah, Anand Kumar Maurya, Bharti Mittal, Jason K D'Silva, Sakthivel Murugan, Lakshmi Mahadevan, Rekha Sathian, V L Ramprasad, Papia Chakraborty, Ravi Gupta, Amitabha Chaudhuri, Arati Khanna-Gupta
المصدر: PLoS ONE, Vol 13, Iss 9, p e0203845 (2018)
وصف الملف: electronic resource
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2دورية أكاديمية
المؤلفون: Srividya Neriyanuri, Rajiv Raman, Pukhraj Rishi, Kumaramanickavel Govindasamy, V L Ramprasad, Tarun Sharma
المصدر: Indian Journal of Ophthalmology, Vol 63, Iss 9, Pp 741-742 (2015)
مصطلحات موضوعية: Linkage analysis, retinoblastoma, prenatal diagnosis, Ophthalmology, RE1-994
وصف الملف: electronic resource
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3دورية أكاديمية
المؤلفون: Kanika Singh, Sunita Bijarnia-Mahay, V. L. Ramprasad, Ratna Dua Puri, Sandhya Nair, Sheetal Sharda, Renu Saxena, Sudha Kohli, Samarth Kulshreshtha, Indrani Ganguli, Kanwal Gujral, Ishwar C. Verma
المصدر: BMC Medical Genetics, Vol 21, Iss 1, Pp 1-15 (2020)
مصطلحات موضوعية: Carrier screening, Cystic fibrosis, Hearing loss, Pompe disease, Asian Indians, Internal medicine, RC31-1245, Genetics, QH426-470
وصف الملف: electronic resource
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4
المؤلفون: V. Manjunath, S. G. Thenral, B. R. Lakshmi, Atchayaram Nalini, A. Bassi, K. Priya Karthikeyan, K. Piyusha, R. Menon, A. Malhotra, L. S. Praveena, R. M. Anjanappa, S. M. Sakthivel Murugan, Kiran Polavarapu, Mainak Bardhan, V. Preethish-Kumar, Seena Vengalil, Saraswati Nashi, S. Sanga, M. Acharya, R. Raju, V. R. Pai, V. L. Ramprasad, R. Gupta
المصدر: Human Mutation. 2023:1-10
مصطلحات موضوعية: Article Subject, Genetics, Genetics (clinical)
وصف الملف: text/xhtml
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5دورية أكاديمية
المؤلفون: Viswanathan Mohan, Venkatesan Radha, Thong T. Nguyen, Eric W. Stawiski, Kanika Bajaj Pahuja, Leonard D. Goldstein, Jennifer Tom, Ranjit Mohan Anjana, Monica Kong-Beltran, Tushar Bhangale, Suresh Jahnavi, Radhakrishnan Chandni, Vijay Gayathri, Paul George, Na Zhang, Sakthivel Murugan, Sameer Phalke, Subhra Chaudhuri, Ravi Gupta, Jingli Zhang, Sam Santhosh, Jeremy Stinson, Zora Modrusan, V. L. Ramprasad, Somasekar Seshagiri, Andrew S. Peterson
المصدر: BMC Medical Genetics, Vol 19, Iss 1, Pp 1-10 (2018)
مصطلحات موضوعية: MODY, Diabetes, Exome, Genomics analysis, NKX6–1, Internal medicine, RC31-1245, Genetics, QH426-470
وصف الملف: electronic resource
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6
المؤلفون: Shweta Mahalingam, Angela Devanboo, Avinash Pradhan, Ashwini Suravaparu, T. Sai Kiranmai, E. Venkataswamy, V. L. Ramprasad, Priya Kadam
المصدر: The Journal of Obstetrics and Gynecology of India. 73:180-182
مصطلحات موضوعية: Obstetrics and Gynecology
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7
المؤلفون: Raja Pramanik, Avinash Upadhyay, Sachin Khurana, Lalit Kumar, Prabhat S. Malik, Sunesh Kumar, M. D. Ray, S. V. S. Deo, Ritu Gupta, Deepshi Thakral, Sanjay Thulkar, V. L. Ramprasad
المصدر: Indian Journal of Medical and Paediatric Oncology. 43:361-368
مصطلحات موضوعية: Oncology, Pediatrics, Perinatology and Child Health
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::1847a91a60b55fdaaf8d6258e3bb8f67
https://doi.org/10.1055/s-0042-1746197 -
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المؤلفون: Abhenil Mittal, S V S Deo, Ajay Gogia, Atul Batra, Akash Kumar, Sandeep Bhoriwal, Koushik Sinha Deb, Ekta Dhamija, V L Ramprasad, Olufunmilayo Olopade, Raja Pramanik
المصدر: Ecancermedicalscience. 16
مصطلحات موضوعية: Cancer Research, Oncology
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9
المؤلفون: Samarth Kulshreshtha, Ranjana Mishra, Deepti Gupta, Ratna Dua Puri, Vibha Jain, Ishwar C. Verma, V. L. Ramprasad, Renu Saxena
المصدر: Mol Syndromol
مصطلحات موضوعية: Genetics, Proband, 0303 health sciences, 030305 genetics & heredity, Brachydactyly, Biology, medicine.disease, Phenotype, Short stature, Robinow syndrome, DNA sequencing, 03 medical and health sciences, Novel Insights from Clinical Practice, medicine, medicine.symptom, Haploinsufficiency, Genetics (clinical), Exome sequencing, 030304 developmental biology
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9fed2357a50d73690eca58339db9cb9a
https://doi.org/10.1159/000505506 -
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المؤلفون: Raman Puri, Anjali Arora, Ratna Dua Puri, Sanghamitra Mishra, Sireesha Movva, Renu Saxena, Jitendra Pal Singh Sawhney, Samarth Kulshrestha, Ishwar C. Verma, Ishpreet K. Biji, Prahlad Balakrishnan, V. L. Ramprasad, Sanika Apte, Nitika Setia
المصدر: Journal of Clinical Lipidology. 14:35-45
مصطلحات موضوعية: Adult, Male, Proband, Apolipoprotein B, Endocrinology, Diabetes and Metabolism, India, Familial hypercholesterolemia, 030204 cardiovascular system & hematology, Genetic analysis, Hyperlipoproteinemia Type II, Genetic Heterogeneity, 03 medical and health sciences, symbols.namesake, Apolipoproteins E, 0302 clinical medicine, Asian People, Internal Medicine, Humans, Medicine, 030212 general & internal medicine, Gene, Aged, Genetics, Sanger sequencing, Nutrition and Dietetics, biology, business.industry, Genetic heterogeneity, PCSK9, High-Throughput Nucleotide Sequencing, Middle Aged, medicine.disease, Receptors, LDL, Apolipoprotein B-100, Mutation, biology.protein, symbols, Female, lipids (amino acids, peptides, and proteins), Proprotein Convertase 9, Cardiology and Cardiovascular Medicine, business