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

by Eva Pinti, Anna Lengyel, Gyorgy Fekete, Iren Haltrich
Published 2020-01-01

Diagnostic difficulties and possibilities of NF1-like syndromes in childhood

by Eva Pinti, Krisztina Nemeth, Krisztina Staub, Anna Lengyel, Gyorgy Fekete, Iren Haltrich
Published 2021-07-01

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

by Artur Beke, Henriett Piko, Iren Haltrich, Veronika Karcagi, Janos Rigo, Maria Judit Molnar, György Fekete
Published 2018-07-01

Evaluation of Organic Wastes as Substrates for Rearing <i>Zophobas morio</i>, <i>Tenebrio molitor</i>, and <i>Acheta domesticus</i> Larvae as Alternative Feed Supplements

by Endre Harsányi, Csaba Juhász Elza Kovács, László Huzsvai, Richárd Pintér, György Fekete, Zsolt István Varga, László Aleksza, Csaba Gyuricza
Published 2020-09-01

One test for all: whole exome sequencing significantly improves the diagnostic yield in growth retarded patients referred for molecular testing for Silver–Russell syndrome

by Robert Meyer, Matthias Begemann, Christian Thomas Hübner, Daniela Dey, Alma Kuechler, Magdeldin Elgizouli, Ulrike Schara, Laima Ambrozaityte, Birute Burnyte, Carmen Schröder, Asmaa Kenawy, Peter Kroisel, Stephanie Demuth, Gyorgy Fekete, Thomas Opladen, Miriam Elbracht, Thomas Eggermann
Published 2021-01-01

Genotype-Phenotype Associations in Patients With Type-1, Type-2, and Atypical NF1 Microdeletions

by Gergely Büki, Gergely Büki, Anna Zsigmond, Márta Czakó, Márta Czakó, Renáta Szalai, Renáta Szalai, Gréta Antal, Viktor Farkas, György Fekete, Dóra Nagy, Márta Széll, Marianna Tihanyi, Béla Melegh, Béla Melegh, Béla Melegh, Kinga Hadzsiev, Kinga Hadzsiev, Judit Bene, Judit Bene, Judit Bene
Published 2021-06-01