Zakaria Z - Search Results

1

Inherited t(9;22) as the cause of DiGeorge syndrome: a case report.

Shuib S, Abdul Latif Z, Abidin NZ, Akmal SN, Zakaria Z. Shuib S, et al. Among authors: zakaria z. Malays J Pathol. 2009 Dec;31(2):133-6. Malays J Pathol. 2009. PMID: 20514857 Free article.

2

Heterogeneous t(4;11) fusion transcripts in two infants with acute lymphoblastic leukemia.

Gill HK, Ten SK, Dhaliwal JS, Moore S, Hassan R, Karim FA, Zakaria Z, Murad S, Mohamed M, Ibrahim HM, Rahman EJ. Gill HK, et al. Among authors: zakaria z. Malays J Pathol. 2004 Dec;26(2):105-10. Malays J Pathol. 2004. PMID: 16329562

3

Interstitial deletion of the distal long arm of chromosome 4, del (4)(q33-q35), in association with paternal balanced translocation.

Mdzin R, Ko C, Abdul Latif Z, Zakaria Z. Mdzin R, et al. Among authors: zakaria z. Singapore Med J. 2008 Nov;49(11):e336-9. Singapore Med J. 2008. PMID: 19037546 Free article.

4

P16INK4a: a potential diagnostic adjunct for prediction of high-grade cervical lesions in liquid-based cytology: with HPV testing and histological correlation.

Wong YP, Abdul Raub SH, Mohd Dali AZ, Kassim F, Visvalingam V, Zakaria Z, Kamaluddin MA, Noor Akmal S. Wong YP, et al. Among authors: zakaria z. Malays J Pathol. 2016 Aug;38(2):93-101. Malays J Pathol. 2016. PMID: 27568665 Free article.

5

Duplication 17p11.2 (Potocki-Lupski Syndrome) in a child with developmental delay.

Shuib S, Saaid NN, Zakaria Z, Ismail J, Abdul Latiff Z. Shuib S, et al. Among authors: zakaria z. Malays J Pathol. 2017 Apr;39(1):77-81. Malays J Pathol. 2017. PMID: 28413209 Free article.

6

Molecular analysis of fragile X syndrome (FXS) among Malaysian patients with developmental disability.

Ali EZ, Yakob Y, Md Desa N, Ishak T, Zakaria Z, Ngu LK, Keng WT. Ali EZ, et al. Among authors: zakaria z. Malays J Pathol. 2017 Aug;39(2):99-106. Malays J Pathol. 2017. PMID: 28866690 Free article.

7

Terminal microdeletion of chromosome 18 in a Malaysian boy characterized with few features of typical 18q- deletion syndrome: a case report.

Ismail A, Ahid F, Thong MK, Zakaria Z. Ismail A, et al. Among authors: zakaria z. J Med Case Rep. 2023 Jun 10;17(1):250. doi: 10.1186/s13256-023-03984-0. J Med Case Rep. 2023. PMID: 37296475 Free PMC article.

8

Expression and mutational analysis of GATA3 in Malaysian breast carcinomas.

Bong PN, Zakaria Z, Muhammad R, Abdullah N, Ibrahim N, Emran NA, Syed Hussain SN. Bong PN, et al. Among authors: zakaria z. Malays J Pathol. 2010 Dec;32(2):117-22. Malays J Pathol. 2010. PMID: 21329183 Free article.

9

Chromosomal 16p microdeletion in Rubinstein-Taybi syndrome detected by oligonucleotide-based array comparative genomic hybridization: a case report.

Mohd Fadley MA, Ismail A, Keong TM, Yusoff NM, Zakaria Z. Mohd Fadley MA, et al. Among authors: zakaria z. J Med Case Rep. 2012 Jan 23;6:30. doi: 10.1186/1752-1947-6-30. J Med Case Rep. 2012. PMID: 22269667 Free PMC article.

10

FISH analysis using PPAR γ-specific probes for detection of PAX8-PPAR γ translocation in follicular thyroid neoplasms.

Sharifah NA, Zakaria Z, Chia WK. Sharifah NA, et al. Among authors: zakaria z. Methods Mol Biol. 2013;952:187-96. doi: 10.1007/978-1-62703-155-4_13. Methods Mol Biol. 2013. PMID: 23100233

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