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Page 1
Sperm mitochondrial mutations as a cause of low sperm motility.
Thangaraj K, Joshi MB, Reddy AG, Rasalkar AA, Singh L. Thangaraj K, et al. Among authors: singh l. J Androl. 2003 May-Jun;24(3):388-92. doi: 10.1002/j.1939-4640.2003.tb02687.x. J Androl. 2003. PMID: 12721215 Free article.
Y chromosome deletions in azoospermic men in India.
Thangaraj K, Gupta NJ, Pavani K, Reddy AG, Subramainan S, Rani DS, Ghosh B, Chakravarty B, Singh L. Thangaraj K, et al. Among authors: singh l. J Androl. 2003 Jul-Aug;24(4):588-97. doi: 10.1002/j.1939-4640.2003.tb02710.x. J Androl. 2003. PMID: 12826698 Free article.
A novel human sex-determining gene linked to Xp11.21-11.23.
Rajender S, Thangaraj K, Gupta NJ, Leelavathy N, Rani DS, Nambiar RG, Kalavathy V, Santhiya ST, Rajangam S, Gopinath PM, Chakravarty B, Singh L. Rajender S, et al. Among authors: singh l. J Clin Endocrinol Metab. 2006 Oct;91(10):4028-36. doi: 10.1210/jc.2006-0950. Epub 2006 Jul 25. J Clin Endocrinol Metab. 2006. PMID: 16868052
Allelic variation in the NPY gene in 14 Indian populations.
Bhaskar LVKS, Thangaraj K, Shah AM, Pardhasaradhi G, Praveen Kumar K, Reddy AG, Papa Rao A, Mulligan CJ, Singh L, Rao VR. Bhaskar LVKS, et al. Among authors: singh l. J Hum Genet. 2007;52(7):592-598. doi: 10.1007/s10038-007-0158-x. Epub 2007 Jun 7. J Hum Genet. 2007. PMID: 17554476
2,048 results