Harteveld CL - Search Results

1

A novel deletion causing alpha thalassemia clarifies the importance of the major human alpha globin regulatory element.

Viprakasit V, Harteveld CL, Ayyub H, Stanley JS, Giordano PC, Wood WG, Higgs DR. Viprakasit V, et al. Among authors: harteveld cl. Blood. 2006 May 1;107(9):3811-2. doi: 10.1182/blood-2005-12-4834. Blood. 2006. PMID: 16627766 Free article. No abstract available.

2

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: harteveld cl. 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.

3

Multiple recombination events are responsible for the heterogeneity of alpha(+)-thalassemia haplotypes among the forest tribes of Andhra Pradesh, India.

Fodde R, Harteveld CL, Losekoot M, Giordano PC, Khan PM, Nayudu NV, Bernini LF. Fodde R, et al. Among authors: harteveld cl. Ann Hum Genet. 1991 Jan;55(1):43-50. doi: 10.1111/j.1469-1809.1991.tb00397.x. Ann Hum Genet. 1991. PMID: 2042935

4

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

5

A novel frameshift mutation [FSC 47 (+A)] causing beta-thalassemia in a Surinam patient.

Losekoot M, Fodde R, van Heeren H, Harteveld CL, Giordano PC, Bernini LF. Losekoot M, et al. Among authors: harteveld cl. Hemoglobin. 1990;14(4):467-70. doi: 10.3109/03630269009032010. Hemoglobin. 1990. PMID: 2283303 No abstract available.

6

Prenatal diagnosis of homozygous alpha zero-thalassemia by an immunological method.

Bernini LF, Kanhai HH, Losekoot M, Giordano P, Harteveld CL. Bernini LF, et al. Among authors: harteveld cl. Ann N Y Acad Sci. 1994 Sep 7;731:193-6. doi: 10.1111/j.1749-6632.1994.tb55769.x. Ann N Y Acad Sci. 1994. PMID: 7944118 No abstract available.

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. 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 Kurdistan [alpha 47(CE5)Asp-->Tyr], a new alpha chain variant in combination with beta (0)-thalassemia.

Giordano PC, Harteveld CL, Streng H, Oosterwijk JC, Heister JG, Amons R, Bernini LF. Giordano PC, et al. Among authors: harteveld cl. Hemoglobin. 1994 Jan;18(1):11-8. doi: 10.3109/03630269409014141. Hemoglobin. 1994. PMID: 8195005

9

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. 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

10

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. 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

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