Krishnamoorthy R - Search Results

1

A novel deletional beta-thalassemic variant in an ethnic Qatari patient.

Al-Obaidli A, Gerard N, Al Zadjali S, Fawzi Z, Pravin S, Pathare A, Krishnamoorthy R. Al-Obaidli A, et al. Among authors: krishnamoorthy r. Hemoglobin. 2009;33(3):214-9. doi: 10.1080/03630260903081398. Hemoglobin. 2009. PMID: 19657835

2

Molecular basis of thalassemia in Qatar.

Al-Obaidli A, Hamodat M, Fawzi Z, Abu-Laban M, Gerard N, Krishnamoorthy R. Al-Obaidli A, et al. Among authors: krishnamoorthy r. Hemoglobin. 2007;31(2):121-7. doi: 10.1080/03630260701288815. Hemoglobin. 2007. PMID: 17486492

3

A novel beta-thalassemia mutation in an Asian Indian.

Shaji RV, Gerard N, Krishnamoorthy R, Srivastava A, Chandy M. Shaji RV, et al. Among authors: krishnamoorthy r. Hemoglobin. 2002 Feb;26(1):49-57. doi: 10.1081/hem-120002940. Hemoglobin. 2002. PMID: 11939512

4

A novel alpha-thalassemia nonsense mutation in codon 23 of the alpha2-globin gene (GAG-->TAG) in a Tunisian family.

Siala H, Fattoum S, Messaoud T, Ouali F, Gerard N, Krishnamoorthy R. Siala H, et al. Among authors: krishnamoorthy r. Hemoglobin. 2004 Aug;28(3):249-54. doi: 10.1081/hem-120040258. Hemoglobin. 2004. PMID: 15481894

5

Present day inbreeding does not forbid the forensic utility of commonly explored STR loci: a case study of native Qataris.

Al-Obaidli A, Sabbagh A, Pravin S, Krishnamoorthy R. Al-Obaidli A, et al. Among authors: krishnamoorthy r. Forensic Sci Int Genet. 2009 Dec;4(1):e11-3. doi: 10.1016/j.fsigen.2008.12.005. Epub 2009 Feb 1. Forensic Sci Int Genet. 2009. PMID: 19948312

6

Forecasting hemoglobinopathy burden through neonatal screening in Omani neonates.

Alkindi S, Al Zadjali S, Al Madhani A, Daar S, Al Haddabi H, Al Abri Q, Gravell D, Berbar T, Pravin S, Pathare A, Krishnamoorthy R. Alkindi S, et al. Among authors: krishnamoorthy r. Hemoglobin. 2010 Jan;34(2):135-44. doi: 10.3109/03630261003677213. Hemoglobin. 2010. PMID: 20353348

7

Molecular spectrum of β-thalassemia mutations in the admixed Venezuelan population, and their linkage to β-globin gene haplotypes.

Bravo-Urquiola M, Arends A, Gómez G, Montilla S, Gerard N, Chacin M, Berbar T, García O, García G, Velasquez D, Castillo O, Krishnamoorthy R. Bravo-Urquiola M, et al. Among authors: krishnamoorthy r. Hemoglobin. 2012;36(3):209-18. doi: 10.3109/03630269.2012.674997. Hemoglobin. 2012. PMID: 22563936

8

Hb A2' (Hb B2) in the Omani population and diagnostic significance.

Daar S, Al Zadjali S, Gravell D, Al Haddabi H, Al Riyami M, Al Belushi A, Berbar T, Krishnamoorthy R. Daar S, et al. Among authors: krishnamoorthy r. Hemoglobin. 2011;35(2):117-24. doi: 10.3109/03630269.2011.553557. Hemoglobin. 2011. PMID: 21417568

9

A new high A2-beta-thalassemia due to a 468 bp deletion (-475 to -8) in the beta-globin gene promoter of the intact beta-globin structural gene.

Kueviakoe I, Gerard N, Krishnamoorthy R, Pereira S, Elion J, Ducrocq R. Kueviakoe I, et al. Among authors: krishnamoorthy r. Hemoglobin. 2004 Feb;28(1):69-72. doi: 10.1081/hem-120028890. Hemoglobin. 2004. PMID: 15008268 No abstract available.

10

Hb Sheffield [β58(E2)Pro→His] in Oman: potential pitfall in genetic counseling.

Al Zadjali S, Daar S, AlKindi S, Gravell D, Al Haddabi H, Berbar T, Krishnamoorthy R. Al Zadjali S, et al. Among authors: krishnamoorthy r. Hemoglobin. 2011;35(2):111-6. doi: 10.3109/03630269.2011.558226. Hemoglobin. 2011. PMID: 21417567

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