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Identification of PKD1 and PKD2 gene variants in a cohort of 125 Asian Indian patients of ADPKD.
Pandita S, Ramachandran V, Balakrishnan P, Rolfs A, Brandau O, Eichler S, Bhalla AK, Khullar D, Amitabh V, Ramanarayanan S, Kher V, Verma J, Kohli S, Saxena R, Verma IC. Pandita S, et al. Among authors: balakrishnan p. J Hum Genet. 2019 May;64(5):409-419. doi: 10.1038/s10038-019-0582-8. Epub 2019 Feb 28. J Hum Genet. 2019. PMID: 30816285 Clinical Trial.
Carrier frequency of F508del mutation of cystic fibrosis in Indian population.
Kapoor V, Shastri SS, Kabra M, Kabra SK, Ramachandran V, Arora S, Balakrishnan P, Deorari AK, Paul VK. Kapoor V, et al. Among authors: balakrishnan p. J Cyst Fibros. 2006 Jan;5(1):43-6. doi: 10.1016/j.jcf.2005.10.002. Epub 2005 Nov 28. J Cyst Fibros. 2006. PMID: 16311077 Free article.
Prenatal diagnosis of megalencephalic leukodystrophy.
Shukla P, Balakrishnan P, Agarwal N, Ghosh M, Kabra M, Sharma R, Deka D, Kalra V. Shukla P, et al. Among authors: balakrishnan p. Prenat Diagn. 2008 Apr;28(4):357-9. doi: 10.1002/pd.1931. Prenat Diagn. 2008. PMID: 18330867 No abstract available.
Gene symbol: ATP7B.
Balakrishnan P, Kabra M, Arora NK, Kalra V. Balakrishnan P, et al. Hum Genet. 2007 Feb;120(6):908. Hum Genet. 2007. PMID: 17438596 No abstract available.
371 results