Fekete G - Search Results

1

Multipoint interphase FISH analysis of chromosome 3 abnormalities in 28 childhood AML patients.

Haltrich I, Kost-Alimova M, Kovács G, Klein G, Fekete G, Imreh S. Haltrich I, et al. Among authors: fekete g. Eur J Haematol. 2006 Feb;76(2):124-33. doi: 10.1111/j.1600-0609.2005.00576.x. Eur J Haematol. 2006. PMID: 16405433

2

[Identification of 3q21q26 syndrome by "multipoint" interphase FISH analyses in childhood myeloid leukemia].

Haltrich I, Kost-Alimova M, Kovács G, Kriván G, Dobos M, Imreh S, Fekete G. Haltrich I, et al. Among authors: fekete g. Magy Onkol. 2005;49(2):141-7. Epub 2005 Oct 24. Magy Onkol. 2005. PMID: 16249810 Free article. Hungarian.

3

Jumping translocation of 17q11 approximately qter and 3q25 approximately q28 duplication in a variant Philadelphia t(9;14;22)(q34;q32;q11) in a childhood chronic myelogenous leukemia.

Haltrich I, Kost-Alimova M, Kovács G, Kriván G, Tamáska J, Klein G, Fekete G, Imreh S. Haltrich I, et al. Among authors: fekete g. Cancer Genet Cytogenet. 2006 Jan 1;164(1):74-80. doi: 10.1016/j.cancergencyto.2005.06.019. Cancer Genet Cytogenet. 2006. PMID: 16364767

4

Multipoint interphase FISH in childhood T-acute lymphoblastic leukemia detects subpopulations that carry different chromosome 3 aberrations.

Haltrich I, Kost-Alimova M, Kovács G, Dobos M, Klein G, Fekete G, Imreh S. Haltrich I, et al. Among authors: fekete g. Cancer Genet Cytogenet. 2007 Jan 1;172(1):54-60. doi: 10.1016/j.cancergencyto.2006.08.004. Cancer Genet Cytogenet. 2007. PMID: 17175380

5

[Intrachromosomal amplification of AML1 gene in childhood acute lymphoblastic leukemia].

Haltrich I, Csóka M, Kovács G, Fekete G. Haltrich I, et al. Among authors: fekete g. Orv Hetil. 2008 Jun 15;149(24):1143-6. doi: 10.1556/OH.2008.28388. Orv Hetil. 2008. PMID: 18539581 Hungarian.

6

[Cytogenetic and FISH findings are complementary in childhood ALL].

Haltrich I, Csóka M, Kovács G, Fekete G. Haltrich I, et al. Among authors: fekete g. Magy Onkol. 2008 Sep;52(3):283-91. doi: 10.1556/MOnkol.52.2008.3.6. Magy Onkol. 2008. PMID: 18845499 Hungarian.

7

Donor-cell myelodysplastic syndrome developing 13 years after marrow grafting for aplastic anemia.

Haltrich I, Müller J, Szabó J, Kovács G, Kóos R, Poros A, Dobos M, Fekete G. Haltrich I, et al. Among authors: fekete g. Cancer Genet Cytogenet. 2003 Apr 15;142(2):124-8. doi: 10.1016/s0165-4608(02)00804-x. Cancer Genet Cytogenet. 2003. PMID: 12699888

8

Six cases of rare gene amplifications and multiple copy of fusion gene in childhood acute lymphoblastic leukemia.

Haltrich I, Csóka M, Kovács G, Török D, Alpár D, Ottoffy G, Fekete G. Haltrich I, et al. Among authors: fekete g. Pathol Oncol Res. 2013 Jan;19(1):123-8. doi: 10.1007/s12253-012-9533-9. Epub 2012 Apr 24. Pathol Oncol Res. 2013. PMID: 22528566 Free article.

9

[Examination of sex chromosome abnormalities in childhood].

Pinti É, Lengyel A, Sallai Á, Fekete G, Haltrich I. Pinti É, et al. Among authors: fekete g. Orv Hetil. 2018 Jul;159(27):1121-1128. doi: 10.1556/650.2018.31081. Orv Hetil. 2018. PMID: 29961370 Hungarian.

10

Clinical and genetic findings in Hungarian pediatric patients carrying chromosome 16p copy number variants and a review of the literature.

Lengyel A, Pinti É, Pikó H, Jávorszky E, David D, Tihanyi M, Gönczi É, Kiss E, Tóth Z, Tory K, Fekete G, Haltrich I. Lengyel A, et al. Among authors: fekete g. Eur J Med Genet. 2020 Oct;63(10):104027. doi: 10.1016/j.ejmg.2020.104027. Epub 2020 Aug 3. Eur J Med Genet. 2020. PMID: 32758661 Free article. Review.

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