Lapouméroulie C - Search Results

1

Four new haplotypes observed in Algerian beta-thalassemia patients.

Beldjord C, Lapouméroulie C, Baird ML, Girot R, Adjrad L, Lenoir G, Benabadji M, Labie D. Beldjord C, et al. Among authors: lapoumeroulie c. Hum Genet. 1983;65(2):204-6. doi: 10.1007/BF00286665. Hum Genet. 1983. PMID: 6317540

2

DNA haplotype distribution in Algerian beta thalassaemia patients. An extended evaluation by family studies and representative molecular characterization.

Rouabhi F, Lapouméroulie C, Amselem S, Krishnamoorthy R, Adjrad L, Girot R, Chardin P, Benabdji M, Labie D, Beldjord C. Rouabhi F, et al. Among authors: lapoumeroulie c. Hum Genet. 1988 Aug;79(4):373-6. doi: 10.1007/BF00282180. Hum Genet. 1988. PMID: 2900801

3

Alpha-globin loci in homozygous beta-thalassemia intermedia.

Triadou P, Lapoumeroulie C, Girot R, Labie D. Triadou P, et al. Among authors: lapoumeroulie c. Hum Genet. 1983;63(4):338-40. doi: 10.1007/BF00274758. Hum Genet. 1983. PMID: 6305827

4

A haplotype-linked four base pair deletion upstream of the A gamma globin gene coincides with decreased gene expression.

Beldjord C, Ducrocq R, Nadifi S, Lapoumeroulie C, Elion J, Labie D. Beldjord C, et al. Among authors: lapoumeroulie c. Hum Genet. 1992 Aug;89(6):625-8. doi: 10.1007/BF00221951. Hum Genet. 1992. PMID: 1355067

5

[Intermediate homozygous beta-thalassemia with high fetal hemoglobin synthesis. Molecular analysis].

Cohen-Haguenauer O, Lapoumeroulie C, Labie D, Girot R. Cohen-Haguenauer O, et al. Among authors: lapoumeroulie c. Presse Med. 1989 Feb 4;18(4):173-6. Presse Med. 1989. PMID: 2466287 French.

6

A novel beta thalassemia gene with a single base mutation in the conserved polypyrimidine sequence at the 3' end of IVS 2.

Beldjord C, Lapoumeroulie C, Pagnier J, Benabadji M, Krishnamoorthy R, Labie D, Bank A. Beldjord C, et al. Among authors: lapoumeroulie c. Nucleic Acids Res. 1988 Jun 10;16(11):4927-35. doi: 10.1093/nar/16.11.4927. Nucleic Acids Res. 1988. PMID: 3387213 Free PMC article.

7

Linkage between fetal A gamma globin chain polymorphism and DNA polymorphism of the human beta gene cluster in beta thalassaemia.

Beldjord C, Arbane M, Lapoumeroulie C, Rouyer-Fessard P, Benabadji M, Labie D, Beuzard Y. Beldjord C, et al. Among authors: lapoumeroulie c. Mol Biol Med. 1984 Aug;2(4):301-6. Mol Biol Med. 1984. PMID: 6100562

8

Inter-ethnic polymorphism of the beta-globin gene locus control region (LCR) in sickle-cell anemia patients.

Périchon B, Ragusa A, Lapouméroulie C, Romand A, Moi P, Ikuta T, Labie D, Elion J, Krishnamoorthy R. Périchon B, et al. Among authors: lapoumeroulie c. Hum Genet. 1993 Jun;91(5):464-8. doi: 10.1007/BF00217773. Hum Genet. 1993. PMID: 8314558

9

High genetic polymorphism of hemoglobin disorders in Laos. Complex phenotypes due to associated thalassemic syndromes.

Sicard D, Lieurzou Y, Lapoumeroulie C, Labie D. Sicard D, et al. Among authors: lapoumeroulie c. Hum Genet. 1979 Sep;50(3):327-36. doi: 10.1007/BF00399399. Hum Genet. 1979. PMID: 489017 No abstract available.

10

Common haplotype dependency of high G gamma-globin gene expression and high Hb F levels in beta-thalassemia and sickle cell anemia patients.

Labie D, Pagnier J, Lapoumeroulie C, Rouabhi F, Dunda-Belkhodja O, Chardin P, Beldjord C, Wajcman H, Fabry ME, Nagel RL. Labie D, et al. Among authors: lapoumeroulie c. Proc Natl Acad Sci U S A. 1985 Apr;82(7):2111-4. doi: 10.1073/pnas.82.7.2111. Proc Natl Acad Sci U S A. 1985. PMID: 2580306 Free PMC article.

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