Poon PM - Search Results

1

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

2

Frequency of the fragile X syndrome in Chinese mentally retarded populations is similar to that in Caucasians.

Zhong N, Ju W, Xu W, Ye L, Shen Y, Wu G, Chen SH, Jin R, Hu XF, Yang A, Liu X, Poon P, Pang C, Zheng Y, Song L, Zhao P, Fu B, Gu H, Brown WT. Zhong N, et al. Am J Med Genet. 1999 May 28;84(3):191-4. doi: 10.1002/(sici)1096-8628(19990528)84:3<191::aid-ajmg3>3.0.co;2-8. Am J Med Genet. 1999. PMID: 10331588

3

AGG interspersion analysis of the FMR1 CGG repeats in mental retardation of unspecific cause.

Poon PM, Chen QL, Zhong N, Lam ST, Lai KY, Wong CK, Pang CP. Poon PM, et al. Clin Biochem. 2006 Mar;39(3):244-8. doi: 10.1016/j.clinbiochem.2005.11.005. Epub 2005 Dec 7. Clin Biochem. 2006. PMID: 16337617

4

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

5

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

6

Rapid analysis of CGG repeat length in the FMR1 gene.

Poon PM, Zhao Z, Wu XQ, Ni YX, Pang CP. Poon PM, et al. Clin Chem Lab Med. 2000 Sep;38(9):935-8. doi: 10.1515/CCLM.2000.137. Clin Chem Lab Med. 2000. PMID: 11097353

7

A survey of FRAXE allele sizes in three populations.

Zhong N, Ju W, Curley D, Wang D, Pietrofesa J, Wu G, Shen Y, Pang C, Poon P, Liu X, Gou S, Kajanoja E, Ryynänen M, Dobkin C, Brown WT. Zhong N, et al. Am J Med Genet. 1996 Aug 9;64(2):415-9. doi: 10.1002/(SICI)1096-8628(19960809)64:2<415::AID-AJMG36>3.0.CO;2-G. Am J Med Genet. 1996. PMID: 8844095

8

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

9

Gas chromatographic-mass fragmentographic determination of serum 1 alpha,25 dihydroxyvitamin D3.

Poon PM, Mak YT, Pang CP. Poon PM, et al. Clin Biochem. 1993 Dec;26(6):461-9. doi: 10.1016/0009-9120(93)80010-r. Clin Biochem. 1993. PMID: 8124861

10

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.

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