Items where Subject is "Genetics (clinical)"

Group by: Item Type | No Grouping
Number of items at this level: 6.

Jacob, Prince and Singh, Swati and Bhavani, Gandham Srilakshmi and Gowrishankar, Kalpana and Narayanan, Dhanya Lakshmi and Nampoothiri, Sheela and Patil, Siddaramappa Jagdish and Soni, Jai Prakash and Muranjan, Mamta N. and Kapoor, Seema and Dhingra, Bhavana and Bhat, Ballambattu Vishnu and Bajaj, Shruti and Banerjee, Amrita and Mamadapur, Mahabaleshwar and Sankar, Vaikom Hariharan and Kamath, Nutan and Shenoy, Rathika Damodara and Suri, Deepti and Shukla, Anju and Dalal, Ashwin Bhikaji and Phadke, Shubha Rao and Nishimura, Gen and Mortier, Geert R. and Shah, Hitesh Hasmukhlal and Girisha, Katta Mohan (2025) Genetic and allelic heterogeneity in 248 Indians with skeletal dysplasia. European Journal of Human Genetics, 33 (5). 607 - 613. ISSN 10184813; 14765438

Jeyakumar, B. and Ambujam, G. and Suganya, K. and Arunagiri, R. (2022) BRCA-1 mediated activation of NF-κβ and its pro-inflammatory network drives tumorigenesis in benign breast disease patients. Human Gene, 33. p. 201060. ISSN 27730441

Murugan, Durga and Babu, Senthil Kumar and Kalaimamani, Ezhil Vendhan and Raju, Kamaraj (2024) Corneal microstructural changes of precise CHST6 gene mutation: a case series. Egyptian Journal of Medical Human Genetics, 25 (1). ISSN 2090-2441

Murugan, Manoranjani and Musib, Sourav and Vetriselvan, Yogesh and Karthiga, Ilangovan and Soccalingam, Artchoudane and Samuel, Melissa Shaelyn and Ganesh, Irisappan and Ravikumar, Sambandam (2025) Genetic variants of leptin receptor gene (rs1137101) and obesity risk in prakriti individuals and its pathogenicity prediction using in silico approaches. Egyptian Journal of Medical Human Genetics, 26 (1). ISSN 11108630; 20902441

Muthu, M. and Jayachandran, D. and Sekar, S.Y. and Md Younus, P. and Venugopal, A. and Suresh Babu, H.W. and Ajay, E. and Sanjana, M. and Narayanasamy, N. and Balachandar, V. (2022) A new insight into the diverse facets of microRNA-31 in oral squamous cell carcinoma. Egyptian Journal of Medical Human Genetics, 23 (1): 149. ISSN 11108630; 20902441

Pai, Anand and Shakir, Mohammad (2013) Mayer-Rokitansky-Kuster-Hauser syndrome type II: A rare case. Indian Journal of Human Genetics, 19 (1). p. 113. ISSN 0971-6866

This list was generated on Tue Jan 20 15:45:01 2026 IST.