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Internal Medicine Journal|April 22, 2011
Prevalence and molecular study of G6PD deficiency in Malaysian Orang AsliF Amini, E Ismail, B-A ZilfalilIndian Journal of Pediatrics|May 29, 2009
Clinical manifestations in trisomy 9T P Kannan, S Hemlatha, R Ankathil, et al.The Medical Journal of Malaysia|August 20, 2019
Clinical and genetic analysis of long QT syndrome in two Malay childrenA R Wong, B A Zilfalil, Z A BhuiyanSingapore Medical Journal|July 26, 2006
A Malay boy with the Cornelia de Lange syndrome: clinical and molecular findingsZ A Bhuiyan, B A Zilfalil, R C M HennekamSingapore Medical Journal|April 25, 2007
Two cases of isochromosome 18q syndromeS Pal, M I Siti, R Ankathil, et al.Singapore Medical Journal|January 7, 2006
Ocular findings in Malaysian children with Down syndromeA T Liza-Sharmini, Z N Azlan, B A ZilfalilSingapore Medical Journal|April 18, 2008
Two cases of deletion 5p syndrome: one with paternal involvement and another with atypical presentationB Z Azman, S M Akhir, B A Zilfalil, et al.Journal of Dental Research|February 8, 2011
Contribution of 6p24 to non-syndromic cleft lip and palate in a Malay population: association of variants in OFC1I Salahshourifar, A S Halim, W A W Sulaiman, et al.Journal of Clinical Pharmacy and Therapeutics|December 9, 2004
Genetic polymorphism of CYP2D6 in patients with cardiovascular disease -- a cohort studyL K Teh, B A Zilfalil, I Marina, et al.The Journal of Laryngology and Otology|March 21, 2008
Screening for gap junction protein beta-2 gene mutations in Malays with autosomal recessive, non-syndromic hearing loss, using denaturing high performance liquid chromatographyZ Siti Aishah, M D Mohd Khairi, A R Normastura, et al.Pageof 3