Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Abnormalities and FANCL[original query] |
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A comprehensive molecular study identified 12 complementation groups with 56 novel FANC gene variants in Indian Fanconi anemia subjects. Human mutation 2021 Sep . George Merin, Solanki Avani, Chavan Niranjan, Rajendran Aruna, Raj Revathi, Mohan Sheila, Nemani Sandeep, Kanvinde Shailesh, Munirathnam Deendayalan, Rao Sudha, Radhakrishnan Nita, Lashkari Harsha Prasada, Ghildhiyal Radha Gulati, Manglani Mamta, Shanmukhaiah Chandrakala, Bhat Sunil, Ramesh Sowmyashree, Cherian Anchu, Junagade Pritesh, Vundinti Babu R |
Nitric oxide synthase-2 (NOS2) gene polymorphism c.1832C>T (Ser608Leu) associated with nitrosative stress in Fanconi anaemia. Molecular biology reports 2021 Mar . George Merin, Solanki Avani, Mohanty Purvi, Dhangar Somprakash, Rajendran Aruna, Mohan Sheila, Vundinti Babu R |
Severe telomere shortening in Fanconi anemia complementation group L. Molecular biology reports 2021 1 48 (1): 585-593. Shah Anjali, George Merin, Dhangar Somprakash, Rajendran Aruna, Mohan Sheila, Vundinti Babu R |
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- Page last updated:Apr 22, 2024
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