Fekete G - Search Results

1

[Clinical aspects of 22q11.2 microdeletion syndrome].

Szumutku F, Kádár K, Kovács ÁF, Lengyel A, Pinti É, Némethi Z, Abonyi T, Csáky-Szunyogh M, Fekete G, Haltrich I. Szumutku F, et al. Among authors: fekete g. Orv Hetil. 2022 Jan 2;163(1):21-30. doi: 10.1556/650.2022.32299. Print 2022 Jan 2. Orv Hetil. 2022. PMID: 34974426 Hungarian.

2

[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.

3

[Trisomy 9p and clinical heterogeneity: case report of an unusual presentation].

Lengyel A, Kosik A, Pinti É, Lódi C, Tory K, Fekete G, Haltrich I. Lengyel A, et al. Among authors: fekete g. Orv Hetil. 2018 Nov;159(47):1994-2000. doi: 10.1556/650.2018.31223. Orv Hetil. 2018. PMID: 30474384 Hungarian.

4

[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.

5

[Williams-Beuren syndrome (Williams syndrome). Case report].

Miklós G, Fekete G, Haltrich I, Tóth M, Reismann P. Miklós G, et al. Among authors: fekete g. Orv Hetil. 2017 Nov;158(47):1883-1888. doi: 10.1556/650.2017.30905. Orv Hetil. 2017. PMID: 29153020 Hungarian.

6

[Rapid first-tier genetic diagnosis in patients with Prader-Willi syndrome].

Ács OD, Péterfia B, Hollósi P, Haltrich I, Sallai Á, Luczay A, Buiting K, Horsthemke B, Török D, Szabó A, Fekete G. Ács OD, et al. Among authors: fekete g. Orv Hetil. 2018 Jan;159(2):64-69. doi: 10.1556/650.2018.30918. Orv Hetil. 2018. PMID: 29307221 Hungarian.

7

Diagnostic difficulties and possibilities of NF1-like syndromes in childhood.

Pinti E, Nemeth K, Staub K, Lengyel A, Fekete G, Haltrich I. Pinti E, et al. Among authors: fekete g. BMC Pediatr. 2021 Jul 29;21(1):331. doi: 10.1186/s12887-021-02791-0. BMC Pediatr. 2021. PMID: 34325699 Free PMC article.

8

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.

9

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.

10

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.

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