Losekoot M - Search Results

1

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. Br J Haematol. 1990 Oct;76(2):269-74. doi: 10.1111/j.1365-2141.1990.tb07883.x. Br J Haematol. 1990. PMID: 2094329

2

A novel 7.9 kb deletion causing alpha+-thalassaemia in two independent families of Indian origin.

Harteveld CL, van Delft P, Wijermans PW, Kappers-Klunne MC, Weegenaar J, Losekoot M, Giordano PC. Harteveld CL, et al. Among authors: losekoot m. Br J Haematol. 2003 Jan;120(2):364-6. doi: 10.1046/j.1365-2141.2003.04060.x. Br J Haematol. 2003. PMID: 12542500 Free article.

3

Rapid detection of the highly polymorphic beta globin framework by denaturing gradient gel electrophoresis.

Losekoot M, van Heeren H, Schipper JJ, Giordano PC, Bernini LF, Fodde R. Losekoot M, et al. J Med Genet. 1992 Aug;29(8):574-7. doi: 10.1136/jmg.29.8.574. J Med Genet. 1992. PMID: 1355561 Free PMC article. No abstract available.

4

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: losekoot m. Br J Haematol. 1992 Apr;80(4):533-8. doi: 10.1111/j.1365-2141.1992.tb04569.x. Br J Haematol. 1992. PMID: 1374633

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. 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: losekoot m. Genomics. 1990 Dec;8(4):732-5. doi: 10.1016/0888-7543(90)90263-t. Genomics. 1990. PMID: 2276746

7

A novel delta zero-thalassemia arising from a frameshift insertion, detected by direct sequencing of enzymatically amplified DNA.

Losekoot M, Fodde R, Giordano PC, Bernini LF. Losekoot M, et al. Hum Genet. 1989 Aug;83(1):75-8. doi: 10.1007/BF00274153. Hum Genet. 1989. PMID: 2767680

8

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: losekoot m. Br J Haematol. 1994 May;87(1):139-43. doi: 10.1111/j.1365-2141.1994.tb04883.x. Br J Haematol. 1994. PMID: 7947237

9

Mutation detection by denaturing gradient gel electrophoresis (DGGE).

Fodde R, Losekoot M. Fodde R, et al. Among authors: losekoot m. Hum Mutat. 1994;3(2):83-94. doi: 10.1002/humu.1380030202. Hum Mutat. 1994. PMID: 8199599 Review.

10

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: losekoot m. 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

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