Gerard N - Search Results

1

Spectrum of beta thalassemia mutations and their linkage to beta-globin gene haplotypes in the Indo-Mauritians.

Kotea N, Ramasawmy R, Lu CY, Fa NS, Gerard N, Beesoon S, Ducrocq R, Surrun SK, Nagel RL, Krishnamoorthy R. Kotea N, et al. Among authors: gerard n. Am J Hematol. 2000 Jan;63(1):11-5. doi: 10.1002/(sici)1096-8652(200001)63:1<11::aid-ajh3>3.0.co;2-d. Am J Hematol. 2000. PMID: 10602161 Free article.

2

Implications of the genetic epidemiology of globin haplotypes linked to the sickle cell gene in southern Iran.

Rahimi Z, Merat A, Gerard N, Krishnamoorthy R, Nagel RL. Rahimi Z, et al. Among authors: gerard n. Hum Biol. 2006 Dec;78(6):719-31. doi: 10.1353/hub.2007.0016. Hum Biol. 2006. PMID: 17564250

3

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: gerard n. Hemoglobin. 2004 Feb;28(1):69-72. doi: 10.1081/hem-120028890. Hemoglobin. 2004. PMID: 15008268 No abstract available.

4

A novel C-->A transversion within the distal CCAAT motif of the Ggamma-globin gene in the Algerian Ggammabeta+-hereditary persistence of fetal hemoglobin.

Zertal-Zidani S, Merghoub T, Ducrocq R, Gerard N, Satta D, Krishnamoorthy R. Zertal-Zidani S, et al. Among authors: gerard n. Hemoglobin. 1999 May;23(2):159-69. doi: 10.3109/03630269908996160. Hemoglobin. 1999. PMID: 10335983

5

A mismatched-primer polymerase chain reaction-restriction fragment length polymorphism strategy for rapid screening of the polyadenylation signal mutation alpha(T-Saudi) (AATAAA-->AATAAG) in the alpha2-globin gene.

Jassim N, Al-Arrayed S, Gerard N, Al-Mukharraq H, Al-Ajami A, Ramasawmy R, Krishnamoorthy R. Jassim N, et al. Among authors: gerard n. Hemoglobin. 1999 Aug;23(3):213-20. doi: 10.3109/03630269909005701. Hemoglobin. 1999. PMID: 10490133

6

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: gerard n. Hemoglobin. 2002 Feb;26(1):49-57. doi: 10.1081/hem-120002940. Hemoglobin. 2002. PMID: 11939512

7

Origin of Hb S Antilles.

Romana M, Gerard N, Chout R, Krishnamoorthy R, Marianne-Pepin T. Romana M, et al. Among authors: gerard n. Am J Hematol. 2002 Aug;70(4):331-2. doi: 10.1002/ajh.10121. Am J Hematol. 2002. PMID: 12210818 Free article. No abstract available.

8

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: gerard n. Hemoglobin. 2004 Aug;28(3):249-54. doi: 10.1081/hem-120040258. Hemoglobin. 2004. PMID: 15481894

9

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: gerard n. Hemoglobin. 2012;36(3):209-18. doi: 10.3109/03630269.2012.674997. Hemoglobin. 2012. PMID: 22563936

10

Mutation frequencies of the cytochrome CYP2D6 gene in Parkinson disease patients and in families.

Lucotte G, Turpin JC, Gérard N, Panserat S, Krishnamoorthy R. Lucotte G, et al. Among authors: gerard n. Am J Med Genet. 1996 Jul 26;67(4):361-5. doi: 10.1002/(SICI)1096-8628(19960726)67:4<361::AID-AJMG8>3.0.CO;2-P. Am J Med Genet. 1996. PMID: 8837703

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