Poon PM - Search Results

1

Novel mitochondrial 16S rRNA mutation, 3200T-->C, associated with adult-onset type 2 diabetes.

Yang T, Lam CW, Tsang MW, Tong SF, Kam GY, Chan LY, Poon PM, Wu X, Pang CP. Yang T, et al. Among authors: poon pm. Chin Med J (Engl). 2002 May;115(5):753-8. Chin Med J (Engl). 2002. PMID: 12133550

2

[Mutation-function analysis in the lipoprotein lipase gene of Chinese patients with hypertriglyceridemic type 2 diabetes].

Yang T, Lam CW, Tsang MW, Chan LY, Poon PM, Huang SZ, Pang CP. Yang T, et al. Among authors: poon pm. Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 2003 Apr;25(2):134-41. Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 2003. PMID: 12905705 Chinese.

3

Novel single nucleotide polymorphisms (3203A>G and 3204C>T) in the 3' end of the mitochondrial 16S rRNA gene.

Yang T, Lam CW, Tsang MW, Tong SF, Chan LY, Kam GY, Poon PM, Wu XQ, Pang CP. Yang T, et al. Among authors: poon pm. Hum Mutat. 2000 Oct;16(4):375. doi: 10.1002/1098-1004(200010)16:4<375::AID-HUMU20>3.0.CO;2-F. Hum Mutat. 2000. PMID: 11013458 No abstract available.

4

Pathogenic mutations of the lipoprotein lipase gene in Chinese patients with hypertriglyceridemic type 2 diabetes.

Yang T, Pang CP, Tsang MW, Lam CW, Poon PM, Chan LY, Wu XQ, Tomlinson B, Baum L. Yang T, et al. Among authors: poon pm. Hum Mutat. 2003 Apr;21(4):453. doi: 10.1002/humu.9134. Hum Mutat. 2003. PMID: 12655575

5

Rapid screening for alpha1-antitrypsin Z and S mutations.

Lam CW, Pang CP, Poon PM, Yin CH, Bharathi G. Lam CW, et al. Among authors: poon pm. Clin Chem. 1997 Feb;43(2):403-4. Clin Chem. 1997. PMID: 9023148 No abstract available.

6

Trinucleotide CGG repeat in the FMR1 gene in Chinese mentally retarded patients.

Pang CP, Poon PM, Chen QL, Lai KY, Yin CH, Zhao Z, Zhong N, Lau CH, Lam ST, Wong CK, Brown WT. Pang CP, et al. Among authors: poon pm. Am J Med Genet. 1999 May 28;84(3):179-83. Am J Med Genet. 1999. PMID: 10331586

7

Novel mutation and polymorphisms of the HMBS gene detected by denaturing HPLC.

Lam CW, Poon PM, Tong SF, Lo AW, Lai CK, Choi KL, Tiu SC, Chan YW, Shek CC. Lam CW, et al. Among authors: poon pm. Clin Chem. 2001 Feb;47(2):343-6. Clin Chem. 2001. PMID: 11159788 No abstract available.

8

Novel splicing mutation of the PPOX gene (IVS10 + 1G-->A) detected by denaturing high-performance liquid chromatography.

Lam CW, Hui KN, Poon PM, Luk NM, Yuen YP, Tong SF, Lai CK, Chan YW, Lo KK. Lam CW, et al. Among authors: poon pm. Clin Chim Acta. 2001 Mar;305(1-2):197-200. doi: 10.1016/s0009-8981(01)00382-5. Clin Chim Acta. 2001. PMID: 11249940 No abstract available.

9

CGG repeat interruptions in the FMR1 gene in patients with infantile autism.

Poon PM, Chen QL, Lai KY, Wong CK, Pang CP. Poon PM, et al. Clin Chem Lab Med. 1998 Aug;36(8):649-53. doi: 10.1515/CCLM.1998.115. Clin Chem Lab Med. 1998. PMID: 9806479

10

FRAXAC1 and DXS548 polymorphisms in the Chinese population.

Poon PM, Pang CP, Chen QL, Zhong N, Lai KY, Lau CH, Wong CK, Brown WT. Poon PM, et al. Am J Med Genet. 1999 May 28;84(3):208-13. doi: 10.1002/(sici)1096-8628(19990528)84:3<208::aid-ajmg8>3.0.co;2-c. Am J Med Genet. 1999. PMID: 10331593

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