Haltrich I - Search Results

1

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. Cancer Genet Cytogenet. 2003 Apr 15;142(2):124-8. doi: 10.1016/s0165-4608(02)00804-x. Cancer Genet Cytogenet. 2003. PMID: 12699888

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. 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. 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 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. Eur J Haematol. 2006 Feb;76(2):124-33. doi: 10.1111/j.1600-0609.2005.00576.x. Eur J Haematol. 2006. PMID: 16405433

5

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. Cancer Genet Cytogenet. 2007 Jan 1;172(1):54-60. doi: 10.1016/j.cancergencyto.2006.08.004. Cancer Genet Cytogenet. 2007. PMID: 17175380

6

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

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

7

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

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

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. 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

Dysfunction of SHANK2 and CHRNA7 in a patient with intellectual disability and language impairment supports genetic epistasis of the two loci.

Chilian B, Abdollahpour H, Bierhals T, Haltrich I, Fekete G, Nagel I, Rosenberger G, Kutsche K. Chilian B, et al. Among authors: haltrich i. Clin Genet. 2013 Dec;84(6):560-5. doi: 10.1111/cge.12105. Epub 2013 Feb 21. Clin Genet. 2013. PMID: 23350639

10

Molecular cytogenetic analysis of Xq critical regions in premature ovarian failure.

Beke A, Piko H, Haltrich I, Csomor J, Matolcsy A, Fekete G, Rigo J, Karcagi V. Beke A, et al. Among authors: haltrich i. Mol Cytogenet. 2013 Dec 20;6(1):62. doi: 10.1186/1755-8166-6-62. Mol Cytogenet. 2013. PMID: 24359613 Free PMC article.

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