Bernini LF - Search Results

1

Rapid identification by denaturing gradient gel electrophoresis of mutations in the gamma-globin gene promoters in non-deletion type HPFH.

Gottardi E, Losekoot M, Fodde R, Saglio G, Camaschella C, Bernini LF. Gottardi E, et al. Among authors: bernini lf. Br J Haematol. 1992 Apr;80(4):533-8. doi: 10.1111/j.1365-2141.1992.tb04569.x. Br J Haematol. 1992. PMID: 1374633

2

Denaturing gradient gel electrophoresis and direct sequencing of PCR amplified genomic DNA: a rapid and reliable diagnostic approach to beta thalassaemia.

Losekoot M, Fodde R, Harteveld CL, van Heeren H, Giordano PC, Bernini LF. Losekoot M, et al. Among authors: bernini lf. Br J Haematol. 1990 Oct;76(2):269-74. doi: 10.1111/j.1365-2141.1990.tb07883.x. Br J Haematol. 1990. PMID: 2094329

3

Detection of K-ras mutations by denaturing gradient gel electrophoresis (DGGE): a study on pancreatic cancer.

Pellegata NS, Losekoot M, Fodde R, Pugliese V, Saccomanno S, Renault B, Bernini LF, Ranzani GN. Pellegata NS, et al. Among authors: bernini lf. Anticancer Res. 1992 Sep-Oct;12(5):1731-5. Anticancer Res. 1992. PMID: 1444240

4

Interaction of two different disorders in the beta-globin gene cluster associated with an increased hemoglobin F production: a novel deletion type of (G) gamma + ((A) gamma delta beta)(0)-thalassemia and a delta(0)-hereditary persistence of fetal hemoglobin determinant.

Losekoot M, Fodde R, Gerritsen EJ, van de Kuit I, Schreuder A, Giordano PC, Vossen JM, Bernini LF. Losekoot M, et al. Among authors: bernini lf. Blood. 1991 Feb 15;77(4):861-7. Blood. 1991. PMID: 1704267 Free article.

5

Homozygous beta+ thalassaemia owing to a mutation in the cleavage-polyadenylation sequence of the human beta globin gene.

Losekoot M, Fodde R, Harteveld CL, van Heeren H, Giordano PC, Went LN, Bernini LF. Losekoot M, et al. Among authors: bernini lf. J Med Genet. 1991 Apr;28(4):252-5. doi: 10.1136/jmg.28.4.252. J Med Genet. 1991. PMID: 1856830 Free PMC article.

6

Nucleotide sequence of the Belgian G gamma+(A gamma delta beta)0-thalassemia deletion breakpoint suggests a common mechanism for a number of such recombination events.

Fodde R, Losekoot M, Casula L, Bernini LF. Fodde R, et al. Among authors: bernini lf. Genomics. 1990 Dec;8(4):732-5. doi: 10.1016/0888-7543(90)90263-t. Genomics. 1990. PMID: 2276746

7

A novel polyadenylation signal mutation in the alpha 2-globin gene causing alpha thalassaemia.

Harteveld CL, Losekoot M, Haak H, Heister GA, Giordano PC, Bernini LF. Harteveld CL, et al. Among authors: bernini lf. Br J Haematol. 1994 May;87(1):139-43. doi: 10.1111/j.1365-2141.1994.tb04883.x. Br J Haematol. 1994. PMID: 7947237

8

Hb Utrecht [alpha 2 129(H12)Leu-->Pro], a new unstable alpha 2-chain variant associated with a mild alpha-thalassaemic phenotype.

Harteveld CL, Giordano PC, Losekoot M, Heister JG, Batelaan D, van Delft P, Bruin MC, Bernini LF. Harteveld CL, et al. Among authors: bernini lf. Br J Haematol. 1996 Sep;94(3):483-5. doi: 10.1046/j.1365-2141.1996.d01-1828.x. Br J Haematol. 1996. PMID: 8790146

9

An IVS1-116 (A-->G) acceptor splice site mutation in the alpha 2 globin gene causing alpha + thalassaemia in two Dutch families.

Harteveld CL, Heister JG, Giordano PC, Batelaan D, von Delft P, Haak HL, Wijermans PW, Losekoot M, Bernini LF. Harteveld CL, et al. Among authors: bernini lf. Br J Haematol. 1996 Dec;95(3):461-6. doi: 10.1046/j.1365-2141.1996.d01-1926.x. Br J Haematol. 1996. PMID: 8943885

10

Atypical HbH disease in a Surinamese patient resulting from a combination of the -SEA and -alpha 3.7 deletions with HbC heterozygosity.

Giordano PC, Harteveld CL, Michiels JJ, Terpstra W, Batelaan D, van Delft P, Plug RJ, van der Wielen MJ, Losekoot M, Bernini LF. Giordano PC, et al. Among authors: bernini lf. Br J Haematol. 1997 Mar;96(4):801-5. doi: 10.1046/j.1365-2141.1997.d01-2093.x. Br J Haematol. 1997. PMID: 9074424 Free article.

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