Hasil Pencarian - Deepa Selvi Rani
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A novel arginine to tryptophan (R144W) mutation in troponin T (cTnT) gene in an indian multigenerational family with dilated cardiomyopathy (FDCM). oleh Deepa Selvi Rani, Perundurai S Dhandapany, Pratibha Nallari, Calambur Narasimhan, Kumarasamy Thangaraj
Diterbitkan 2014-01-01Dapatkan teks lengkap
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Genetic affinities of the central Indian tribal populations. oleh Gunjan Sharma, Rakesh Tamang, Ruchira Chaudhary, Vipin Kumar Singh, Anish M Shah, Sharath Anugula, Deepa Selvi Rani, Alla G Reddy, Muthukrishnan Eaaswarkhanth, Gyaneshwer Chaubey, Lalji Singh, Kumarasamy Thangaraj
Diterbitkan 2012-01-01Dapatkan teks lengkap
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Novel Mutations in β-MYH7 Gene in Indian Patients With Dilated Cardiomyopathy oleh Deepa Selvi Rani, PhD, Archana Vijaya Kumar, PhD, Pratibha Nallari, PhD, Katakam Sampathkumar, PhD, Perundurai S. Dhandapany, PhD, Calambur Narasimhan, MD, Andiappan Rathinavel, MD, Kumarasamy Thangaraj, PhD
Diterbitkan 2022-01-01Dapatkan teks lengkap
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Genetic structure of Tibeto-Burman populations of Bangladesh: evaluating the gene flow along the sides of Bay-of-Bengal. oleh Nurun Nahar Gazi, Rakesh Tamang, Vipin Kumar Singh, Ahmed Ferdous, Ajai Kumar Pathak, Mugdha Singh, Sharath Anugula, Pandichelvam Veeraiah, Subburaj Kadarkaraisamy, Brijesh Kumar Yadav, Alla G Reddy, Deepa Selvi Rani, Syed Saleheen Qadri, Lalji Singh, Gyaneshwer Chaubey, Kumarasamy Thangaraj
Diterbitkan 2013-01-01Dapatkan teks lengkap
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The phylogeography of Y-chromosome haplogroup h1a1a-m82 reveals the likely Indian origin of the European Romani populations. oleh Niraj Rai, Gyaneshwer Chaubey, Rakesh Tamang, Ajai Kumar Pathak, Vipin Kumar Singh, Monika Karmin, Manvendra Singh, Deepa Selvi Rani, Sharath Anugula, Brijesh Kumar Yadav, Ashish Singh, Ramkumar Srinivasagan, Anita Yadav, Manju Kashyap, Sapna Narvariya, Alla G Reddy, George van Driem, Peter A Underhill, Richard Villems, Toomas Kivisild, Lalji Singh, Kumarasamy Thangaraj
Diterbitkan 2012-01-01Dapatkan teks lengkap
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Mutations in the β-Tubulin Gene TUBB5 Cause Microcephaly with Structural Brain Abnormalities oleh Martin Breuss, Julian Ik-Tsen Heng, Karine Poirier, Guoling Tian, Xavier Hubert Jaglin, Zhengdong Qu, Andreas Braun, Thomas Gstrein, Linh Ngo, Matilda Haas, Nadia Bahi-Buisson, Marie-Laure Moutard, Sandrine Passemard, Alain Verloes, Pierre Gressens, Yunli Xie, Kathryn J.H. Robson, Deepa Selvi Rani, Kumarasamy Thangaraj, Tim Clausen, Jamel Chelly, Nicholas Justin Cowan, David Anthony Keays
Diterbitkan 2012-12-01Dapatkan teks lengkap
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“Like sugar in milk”: reconstructing the genetic history of the Parsi population oleh Gyaneshwer Chaubey, Qasim Ayub, Niraj Rai, Satya Prakash, Veena Mushrif-Tripathy, Massimo Mezzavilla, Ajai Kumar Pathak, Rakesh Tamang, Sadaf Firasat, Maere Reidla, Monika Karmin, Deepa Selvi Rani, Alla G. Reddy, Jüri Parik, Ene Metspalu, Siiri Rootsi, Kurush Dalal, Shagufta Khaliq, Syed Qasim Mehdi, Lalji Singh, Mait Metspalu, Toomas Kivisild, Chris Tyler-Smith, Richard Villems, Kumarasamy Thangaraj
Diterbitkan 2017-06-01Dapatkan teks lengkap
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