Yam I - Search Results

1

Linkage of malignant hyperthermia and hyperkalemic periodic paralysis to the adult skeletal muscle sodium channel (SCN4A) gene in a large pedigree.

Moslehi R, Langlois S, Yam I, Friedman JM. Moslehi R, et al. Among authors: yam i. Am J Med Genet. 1998 Feb 26;76(1):21-7. Am J Med Genet. 1998. PMID: 9508059

2

Uniparental disomy for chromosome 16 in humans.

Kalousek DK, Langlois S, Barrett I, Yam I, Wilson DR, Howard-Peebles PN, Johnson MP, Giorgiutti E. Kalousek DK, et al. Among authors: yam i. Am J Hum Genet. 1993 Jan;52(1):8-16. Am J Hum Genet. 1993. PMID: 8434609 Free PMC article.

3

Parental origin of triploidy in human fetuses: evidence for genomic imprinting.

McFadden DE, Kwong LC, Yam IY, Langlois S. McFadden DE, et al. Among authors: yam iy. Hum Genet. 1993 Nov;92(5):465-9. doi: 10.1007/BF00216452. Hum Genet. 1993. PMID: 7902318

4

Single nucleotide polymorphisms of the factor IX gene for linkage analysis in the southern Chinese population.

Chan V, Yam I, Yip B, Au P, Shing MK, Li CK, Chan TK. Chan V, et al. Among authors: yam i. Br J Haematol. 2000 Nov;111(2):540-3. doi: 10.1046/j.1365-2141.2000.02384.x. Br J Haematol. 2000. PMID: 11122097 Free article.

5

Molecular defects in haemophilia B: detection by direct restriction enzyme analysis.

Chan VV, Yip B, Tong TM, Chan TP, Lau K, Yam I, Chan TK. Chan VV, et al. Among authors: yam i. Br J Haematol. 1991 Sep;79(1):63-9. doi: 10.1111/j.1365-2141.1991.tb08008.x. Br J Haematol. 1991. PMID: 1680373

6

A reverse dot-blot method for rapid detection of non-deletion alpha thalassaemia.

Chan V, Yam I, Chen FE, Chan TK. Chan V, et al. Among authors: yam i. Br J Haematol. 1999 Mar;104(3):513-5. doi: 10.1046/j.1365-2141.1999.01221.x. Br J Haematol. 1999. PMID: 10086788 Free article.

7

Carrier incidence for spinal muscular atrophy in southern Chinese.

Chan V, Yip B, Yam I, Au P, Lin CK, Wong V, Chan TK. Chan V, et al. Among authors: yam i. J Neurol. 2004 Sep;251(9):1089-93. doi: 10.1007/s00415-004-0487-z. J Neurol. 2004. PMID: 15372251

8

Detection of paternal alleles in maternal plasma for non-invasive prenatal diagnosis of beta-thalassemia: a feasibility study in southern Chinese.

Chan K, Yam I, Leung KY, Tang M, Chan TK, Chan V. Chan K, et al. Among authors: yam i. Eur J Obstet Gynecol Reprod Biol. 2010 May;150(1):28-33. doi: 10.1016/j.ejogrb.2010.02.016. Epub 2010 Mar 4. Eur J Obstet Gynecol Reprod Biol. 2010. PMID: 20206431

9

Experience in preimplantation genetic diagnosis for exclusion of homozygous alpha degrees thalassemia.

Chan V, Ng EH, Yam I, Yeung WS, Ho PC, Chan TK. Chan V, et al. Among authors: yam i. Prenat Diagn. 2006 Nov;26(11):1029-36. doi: 10.1002/pd.1550. Prenat Diagn. 2006. PMID: 16941716

10

A comprehensive HBV array for the detection of HBV mutants and genotype.

Chan K, Yam I, Yuen J, Yuen MF, Lai CL, Alexander GJ, Chan TK, Chan V. Chan K, et al. Among authors: yam i. Clin Biochem. 2011 Oct;44(14-15):1253-60. doi: 10.1016/j.clinbiochem.2011.07.014. Epub 2011 Aug 6. Clin Biochem. 2011. PMID: 21851814

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