Ankathil R - Search Results

1

Screening of dystrophin gene deletions in Malaysian patients with Duchenne muscular dystrophy.

Marini M, Salmi AA, Watihayati MS, SMardziah MD, Zahri MK, Hoh BP, Ankathil R, Lai PS, Zilfalil BA. Marini M, et al. Among authors: ankathil r. Med J Malaysia. 2008 Mar;63(1):31-4. Med J Malaysia. 2008. PMID: 18935728 Free article.

2

Two cases of isochromosome 18q syndrome.

Pal S, Siti MI, Ankathil R, Zilfalil BA. Pal S, et al. Among authors: ankathil r. Singapore Med J. 2007 May;48(5):e146-50. Singapore Med J. 2007. PMID: 17453088 Free article.

3

Cytogenetic and clinical profile of Down syndrome in Northeast Malaysia.

Azman BZ, Ankathil R, Siti Mariam I, Suhaida MA, Norhashimah M, Tarmizi AB, Nor Atifah MA, Kannan TP, Zilfalil BA. Azman BZ, et al. Among authors: ankathil r. Singapore Med J. 2007 Jun;48(6):550-4. Singapore Med J. 2007. PMID: 17538755 Free article.

4

Two cases of deletion 5p syndrome: one with paternal involvement and another with atypical presentation.

Azman BZ, Akhir SM, Zilfalil BA, Ankathil R. Azman BZ, et al. Among authors: ankathil r. Singapore Med J. 2008 Apr;49(4):e98-e100. Singapore Med J. 2008. PMID: 18418516 Free article. Review.

5

Clinical manifestations in trisomy 9.

Kannan TP, Hemlatha S, Ankathil R, Zilfalil BA. Kannan TP, et al. Among authors: ankathil r. Indian J Pediatr. 2009 Jul;76(7):745-6. doi: 10.1007/s12098-009-0158-2. Epub 2009 May 27. Indian J Pediatr. 2009. PMID: 19475342

6

Chromosomal abnormalities and reproductive outcome in Malaysian couples with miscarriages.

Pal S, Ma SO, Norhasimah M, Suhaida MA, Siti Mariam I, Ankathil R, Zilfalil BA. Pal S, et al. Among authors: ankathil r. Singapore Med J. 2009 Oct;50(10):1008-12. Singapore Med J. 2009. PMID: 19907893 Free article.

7

A new method for FMR1 gene methylation screening by multiplex methylation-specific real-time polymerase chain reaction.

Elias MH, Ankathil R, Salmi AR, Sudhikaran W, Limprasert P, Zilfalil BA. Elias MH, et al. Among authors: ankathil r. Genet Test Mol Biomarkers. 2011 Jun;15(6):387-93. doi: 10.1089/gtmb.2010.0191. Epub 2011 Feb 17. Genet Test Mol Biomarkers. 2011. PMID: 21329465

8

Somatic copy-neutral loss of heterozygosity and copy number abnormalities in Malaysian sporadic colorectal carcinoma patients.

Yam YY, Hoh BP, Othman NH, Hassan S, Yahya MM, Zakaria Z, Ankathil R. Yam YY, et al. Among authors: ankathil r. Genet Mol Res. 2013 Feb 7;12(1):319-27. doi: 10.4238/2013.February.7.1. Genet Mol Res. 2013. PMID: 23420356 Free article.

9

Germline mutation analysis of MLH1 and MSH2 in Malaysian Lynch syndrome patients.

Zahary MN, Kaur G, Abu Hassan MR, Singh H, Naik VR, Ankathil R. Zahary MN, et al. Among authors: ankathil r. World J Gastroenterol. 2012 Feb 28;18(8):814-20. doi: 10.3748/wjg.v18.i8.814. World J Gastroenterol. 2012. PMID: 22371642 Free PMC article.

10

Association of Arg72Pro of P53 polymorphism with colorectal cancer susceptibility risk in Malaysian population.

Aizat AA, Shahpudin SN, Mustapha MA, Zakaria Z, Sidek AS, Abu Hassan MR, Ankathil R. Aizat AA, et al. Among authors: ankathil r. Asian Pac J Cancer Prev. 2011;12(11):2909-13. Asian Pac J Cancer Prev. 2011. PMID: 22393962 Free article.

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