Diagnostic difficulties and possibilities of NF1-like syndromes in childhood von Pinti, Eva, Nemeth, Krisztina, Staub, Krisztina, Lengyel, Anna, Fekete, Gyorgy, Haltrich, Iren

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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 von Pinti, Eva, Lengyel, Anna, Fekete, Gyorgy, Haltrich, Iren

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Deletion of 16q22.2q23.3 in a Boy with a Phenotype Reminiscent of Silver-Russell Syndrome von Lengyel, Anna, Pinti, Éva, Eggermann, Thomas, Fekete, György, Haltrich, Irén

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Microdeletions in 1q21 and 8q12.1 depict two additional molecular subgroups of Silver-Russell syndrome like phenotypes von Baba, Naomi, Lengyel, Anna, Pinti, Eva, Yapici, Elzem, Schreyer, Isolde, Liehr, Thomas, Fekete, György, Eggermann, Thomas

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Clinical and genetic findings in Hungarian pediatric patients carrying chromosome 16p copy number variants and a review of the literature von Lengyel, Anna, Pinti, Éva, Pikó, Henriett, Jávorszky, Eszter, David, Dezső, Tihanyi, Mariann, Gönczi, Éva, Kiss, Eszter, Tóth, Zsuzsa, Tory, Kálmán, Fekete, György, Haltrich, Irén

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An Ultra-Rare Manifestation of an X-Linked Recessive Disorder: Duchenne Muscular Dystrophy in a Female Patient von Szűcs, Zsuzsanna, Pinti, Éva, Haltrich, Irén, Szén, Orsolya Pálné, Nagy, Tibor, Barta, Endre, Méhes, Gábor, Bidiga, László, Török, Olga, Ujfalusi, Anikó, Koczok, Katalin, Balogh, István

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Clinical evaluation of rare copy number variations identified by chromosomal microarray in a Hungarian neurodevelopmental disorder patient cohort von Lengyel, Anna, Pinti, Éva, Pikó, Henriett, Kristóf, Árvai, Abonyi, Tünde, Némethi, Zaránd, Fekete, György, Haltrich, Irén

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Chromosome 2q14.3 microdeletion encompassing CNTNAP5 gene in a patient carrying a complex chromosomal rearrangement von Lengyel, Anna, Pinti, Éva, Nebral, Karin, Pikó, Henriett, Ujfalusi, Anikó, Haas, Oskar A., Fekete, György, Haltrich, Irén

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A Cross-Sectional Study of the Dermatological Manifestations of Patients with Fabry Disease and the Assessment of Angiokeratomas with Multimodal Imaging von Anker, Pálma, Fésűs, Luca, Kiss, Norbert, Lengyel, Anna, Pinti, Éva, Lihacova, Ilze, Lihachev, Alexey, Plorina, Emilija Vija, Fekete, György, Medvecz, Márta

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Similar Cause, Different Phenotype: SOX9 Enhancer Duplication in a Family von Pinti, Eva, Piko, Henriett, Lengyel, Anna, Luczay, Andrea, Karcagi, Veronika, Fekete, Gyorgy, Haltrich, Iren

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Frequency of KCNQ1 variants causing loss of methylation of Imprinting Centre 2 in Beckwith-Wiedemann syndrome von Eßinger, Carla, Karch, Stephanie, Moog, Ute, Fekete, György, Lengyel, Anna, Pinti, Eva, Eggermann, Thomas, Begemann, Matthias

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Diagnostic Use of Genome Sequencing in Patients With 11p15.5 Imprinting Disorder Features: A Pilot Study von Kessler, Luise, Krause, Jeremias, Kraft, Florian, Amin, Asmaa K, Fekete, Gyorgy, Lengyel, Anna, Pinti, Eva, Kovacs, Arpad, Lischka, Annette, Eggermann, Katja, Kurth, Ingo, Knopp, Cordula, Elbracht, Miriam, Begemann, Matthias, Eggermann, Thomas

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Additional file 3 of Clinical evaluation of rare copy number variations identified by chromosomal microarray in a Hungarian neurodevelopmental disorder patient cohort von Lengyel, Anna, Pinti, Éva, Pikó, Henriett, Kristóf, Árvai, Abonyi, Tünde, Némethi, Zaránd, Fekete, György, Haltrich, Irén

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AROMASICHERUNGSKLAMMERVORRICHTUNG ZUM VERSCHLIESSEN VON PAPPBEHÄLTERN von PINTI, EVA

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AROMA-PRESERVING CLIP DEVICE FOR CLOSING CARDBOARD CONTAINERS von PINTI, EVA

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AROMA-PRESERVING CLIP DEVICE FOR CLOSING CARDBOARD CONTAINERS von PINTI, EVA

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AROMA-PRESERVING CLIP DEVICE FOR CLOSING TETRAREX®-TYPE CONTAINERS von PINTI, EVA

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MOLLETTA SALVA-AROMA PER RICHIUDERE CONTENITORI DI TIPO TETRAREX von PINTI EVA

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Deletion of 16q22.2q23.3 in a Boy with a Phenotype Reminiscent of Silver-Russell Syndrome von Lengyel, Anna, Pinti, Éva, Eggermann, Thomas, Fekete, György, Haltrich, Irén

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