Fekete G - Search Results

1

Chromosome 2q14.3 microdeletion encompassing CNTNAP5 gene in a patient carrying a complex chromosomal rearrangement.

Lengyel A, Pinti É, Nebral K, Pikó H, Ujfalusi A, Haas OA, Fekete G, Haltrich I. Lengyel A, et al. Among authors: fekete g. J Genet. 2021;100:66. J Genet. 2021. PMID: 34553698 Free article.

2

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.

3

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

4

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

5

[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.

6

Complex X chromosome rearrangement associated with multiorgan autoimmunity.

Haltrich I, Pikó H, Pamjav H, Somogyi A, Völgyi A, David D, Beke A, Garamvölgyi Z, Kiss E, Karcagi V, Fekete G. Haltrich I, et al. Among authors: fekete g. Mol Cytogenet. 2015 Jul 19;8:51. doi: 10.1186/s13039-015-0152-5. eCollection 2015. Mol Cytogenet. 2015. PMID: 26191082 Free PMC article.

7

[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.

8

Study of patterns of inheritance of premature ovarian failure syndrome carrying maternal and paternal premutations.

Beke A, Piko H, Haltrich I, Karcagi V, Rigo J Jr, Molnar MJ, Fekete G. Beke A, et al. Among authors: fekete g. BMC Med Genet. 2018 Jul 9;19(1):113. doi: 10.1186/s12881-018-0634-5. BMC Med Genet. 2018. PMID: 29986653 Free PMC article.

9

Similar Cause, Different Phenotype: SOX9 Enhancer Duplication in a Family.

Pinti E, Piko H, Lengyel A, Luczay A, Karcagi V, Fekete G, Haltrich I. Pinti E, et al. Among authors: fekete g. Horm Res Paediatr. 2019;92(5):335-339. doi: 10.1159/000503299. Epub 2019 Oct 29. Horm Res Paediatr. 2019. PMID: 31661700

10

What should we consider in the case of combined Down- and 47,XY,+i(X)(q10) Klinefelter syndromes? The unique case of a male newborn and review of the literature.

Pinti E, Lengyel A, Fekete G, Haltrich I. Pinti E, et al. Among authors: fekete g. BMC Pediatr. 2020 Jan 13;20(1):17. doi: 10.1186/s12887-019-1905-9. BMC Pediatr. 2020. PMID: 31931754 Free PMC article. Review.

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