Items where Subject is "Genetics & Heredity"

Group by: Item Type | No Grouping
Number of items at this level: 10.

Jacob, Prince and Singh, Swati and Bhavani, Gandham SriLakshmi and Gowrishankar, Kalpana and Narayanan, Dhanya Lakshmi and Nampoothiri, Sheela and Patil, S. J. and Soni, J. P. and Muranjan, Mamta and Kapoor, Seema and Dhingra, Bhavna and Bhat, Ballambattu Vishnu and Bajaj, Shruti and Banerjee, Amrita and Mamadapur, Mahabaleshwar and Hariharan, Sankar V. and Kamath, Nutan and Shenoy, Rathika D. and Suri, Deepti and Shukla, Anju and Dalal, Ashwin and Phadke, Shubha R. and Nishimura, Gen and Mortier, Geert and Shah, Hitesh and Girisha, Katta M. (2025) Genetic and allelic heterogeneity in 248 Indians with skeletal dysplasia. EUROPEAN JOURNAL OF HUMAN GENETICS, 33.0 (5). pp. 607-613. ISSN 1018-4813

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

Kavitha, M. and Jayachandran, D. and Aishwarya, S. Y. and Younus, P. Md and Venugopal, A. and Babu, H. W. Suresh and Ajay, E. and Sanjana, M. and Arul, 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, 23.0 (1). ISSN 1110-8630

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, 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, 25.0 (1). ISSN 1110-8630

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

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, 26.0 (1). ISSN 1110-8630

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

Vetriselvan, Yogesh and Manoharan, Aarthi and Murugan, Manoranjani and Jayakumar, Swetha and Govindasamy, Chandramohan and Ravikumar, Sambandam (2025) In Silico Characterization of Pathogenic Homeodomain Missense Mutations in the PITX2 Gene. Biochemical Genetics, 63 (3). 2489 - 2512. ISSN 15734927; 00062928

Vetriselvan, Yogesh and Manoharan, Aarthi and Murugan, Manoranjani and Jayakumar, Swetha and Govindasamy, Chandramohan and Ravikumar, Sambandam (2025) In Silico Characterization of Pathogenic Homeodomain Missense Mutations in the PITX2 Gene. BIOCHEMICAL GENETICS, 63.0 (3). pp. 2489-2512. ISSN 0006-2928

This list was generated on Fri Mar 13 21:54:25 2026 IST.