Law HY - Search Results

1

alpha-Thalassemia mutation analyses in Mazandaran province, North Iran.

Tamaddoni A, Hadavi V, Nejad NH, Khosh-Ain A, Siami R, Aghai-Meibodi J, Almadani N, Oberkanins C, Law HY, Najmabadi H. Tamaddoni A, et al. Among authors: law hy. Hemoglobin. 2009;33(2):115-23. doi: 10.1080/03630260902817297. Hemoglobin. 2009. PMID: 19373587

2

Elucidating the spectrum of alpha-thalassemia mutations in Iran.

Hadavi V, Taromchi AH, Malekpour M, Gholami B, Law HY, Almadani N, Afroozan F, Sahebjam F, Pajouh P, Kariminejad R, Kariminejad MH, Azarkeivan A, Jafroodi M, Tamaddoni A, Puehringer H, Oberkanins C, Najmabadi H. Hadavi V, et al. Among authors: law hy. Haematologica. 2007 Jul;92(7):992-3. doi: 10.3324/haematol.10658. Haematologica. 2007. PMID: 17606454 Free article.

3

alpha-thalassemia mutations in Khuzestan Province, Southwest Iran.

Zandian K, Nateghi J, Keikhaie B, Pedram M, Hafezi-Nejad N, Hadavi V, Oberkanins C, Azarkeivan A, Law HY, Najmabadi H. Zandian K, et al. Among authors: law hy. Hemoglobin. 2008;32(6):546-52. doi: 10.1080/03630260802532780. Hemoglobin. 2008. PMID: 19065332

4

Alpha-thalassemia mutations in Gilan Province, North Iran.

Hadavi V, Jafroodi M, Hafezi-Nejad N, Moghadam SD, Eskandari F, Tarashohi S, Pourfahim H, Oberkanins C, Law HY, Najmabadi H. Hadavi V, et al. Among authors: law hy. Hemoglobin. 2009;33(3):235-41. doi: 10.1080/03630260903089029. Hemoglobin. 2009. PMID: 19657838

5

alpha-globin gene deletion and point mutation analysis among in Iranian patients with microcytic hypochromic anemia.

Garshasbi M, Oberkanins C, Law HY, Neishabury M, Kariminejad R, Najmabadi H. Garshasbi M, et al. Among authors: law hy. Haematologica. 2003 Oct;88(10):1196-7. Haematologica. 2003. PMID: 14555321 Review.

6

Validation of a reverse-hybridization StripAssay for the simultaneous analysis of common alpha-thalassemia point mutations and deletions.

Puehringer H, Najmabadi H, Law HY, Krugluger W, Viprakasit V, Pissard S, Baysal E, Taher A, Farra C, Al-Ali A, Al-Ateeq S, Oberkanins C. Puehringer H, et al. Among authors: law hy. Clin Chem Lab Med. 2007;45(5):605-10. doi: 10.1515/CCLM.2007.125. Clin Chem Lab Med. 2007. PMID: 17484620

7

Determining the cause of patchwork HBA1 and HBA2 genes: recurrent gene conversion or crossing over fixation events.

Law HY, Luo HY, Wang W, Ho JF, Najmabadi H, Ng IS, Steinberg MH, Chui DH, Chong SS. Law HY, et al. Haematologica. 2006 Mar;91(3):297-302. Epub 2006 Feb 17. Haematologica. 2006. PMID: 16503550

8

FMR1 CGG repeat patterns and flanking haplotypes in three Asian populations and their relationship with repeat instability.

Zhou Y, Tang K, Law HY, Ng IS, Lee CG, Chong SS. Zhou Y, et al. Among authors: law hy. Ann Hum Genet. 2006 Nov;70(Pt 6):784-96. doi: 10.1111/j.1469-1809.2006.00265.x. Ann Hum Genet. 2006. PMID: 17044853

9

Defining the performance parameters of a rapid screening tool for myotonic dystrophy type 1 based on triplet-primed PCR and melt curve analysis.

Lian M, Law HY, Lee CG, Chong SS. Lian M, et al. Among authors: law hy. Expert Rev Mol Diagn. 2016 Nov;16(11):1221-1232. doi: 10.1080/14737159.2016.1241145. Epub 2016 Oct 8. Expert Rev Mol Diagn. 2016. PMID: 27665623

10

The simultaneous presence of alpha- and beta-thalassaemia alleles: a pitfall of thalassaemia screening.

Law HY, Chee MK, Tan GP, Ng IS. Law HY, et al. Community Genet. 2003;6(1):14-21. doi: 10.1159/000069539. Community Genet. 2003. PMID: 12748434

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