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

5

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

6

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.

7

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

8

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

9

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

10

Contribution to the description of the beta-thalassemia spectrum in Tunisia and the origin of mutation diversity.

Chouk I, Daoud BB, Mellouli F, Bejaoui M, Gérard N, Dellagi K, Abbes S. Chouk I, et al. Among authors: gerard n. Hemoglobin. 2004 Aug;28(3):189-95. doi: 10.1081/hem-120040305. Hemoglobin. 2004. PMID: 15481885

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