Clinical and genetic characteristics of craniosynostosis in Hungary
Bessenyei, Beáta, Nagy, Andrea, Szakszon, Katalin, Mokánszki, Attila, Balogh, Erzsébet, Ujfalusi, Anikó, Tihanyi, Mariann, Novák, László, Bognár, László, Oláh, Éva
Published in American journal of medical genetics. Part A (01.12.2015)
Published in American journal of medical genetics. Part A (01.12.2015)
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Lissencephaly and band heterotopia: LIS1, TUBA1A, and DCX mutations in Hungary
Mokánszki, Attila, Körhegyi, Ivett, Szabó, Nóra, Bereg, Edit, Gergev, Gyurgyinka, Balogh, Erzsébet, Bessenyei, Beáta, Sümegi, Andrea, Morris-Rosendahl, Deborah J, Sztriha, László, Oláh, Eva
Published in Journal of child neurology (01.12.2012)
Published in Journal of child neurology (01.12.2012)
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Correlation study between sperm concentration, hyaluronic acid-binding capacity and sperm aneuploidy in Hungarian patients
Mokánszki, Attila, Molnár, Zsuzsanna, Ujfalusi, Anikó, Balogh, Erzsébet, Bazsáné, Zsuzsa Kassai, Varga, Attila, Jakab, Attila, Oláh, Éva
Published in Reproductive biomedicine online (01.12.2012)
Published in Reproductive biomedicine online (01.12.2012)
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Achondroplasia with multiple-suture craniosynostosis: A report of a new case of this rare association
Bessenyei, Beáta, Nagy, Andrea, Balogh, Erzsébet, Novák, László, Bognár, László, Knegt, Alida C., Oláh, Éva
Published in American journal of medical genetics. Part A (01.10.2013)
Published in American journal of medical genetics. Part A (01.10.2013)
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Dark and Strong?! The associations between dark personality traits, mental toughness and resilience in Hungarian student, employee, leader, and military samples
Szabó, Zsolt Péter, Kun, Ágota, Balogh, Blanka Erzsébet, Simon, Evelin, Csike, Tekla
Published in Personality and individual differences (01.02.2022)
Published in Personality and individual differences (01.02.2022)
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A patient with Smith–Lemli–Opitz syndrome: novel mutation of the DHCR7 gene and effects of therapy with simvastatin and cholesterol supplement
Szabó, Gabriella P., Oláh, Anna V., Kozak, Libor, Balogh, Erzsébet, Nagy, Andrea, Blahakova, Ivona, Oláh, Éva
Published in European journal of pediatrics (2010)
Published in European journal of pediatrics (2010)
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Subtelomeric 6.7 Mb trisomy 10p and 5.6 Mb monosomy 21q detected by FISH and array‐CGH in three related patients
Szabó, Gabriella P., Knegt, Alida C., Ujfalusi, Anikó, Balogh, Erzsébet, Szabó, Tamás, Oláh, Éva
Published in American journal of medical genetics. Part A (01.04.2012)
Published in American journal of medical genetics. Part A (01.04.2012)
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Subtelomeric 6.7Mb trisomy 10p and 5.6Mb monosomy 21q detected by FISH and array-CGH in three related patients
Szabo, Gabriella P, Knegt, Alida C, Ujfalusi, Anikó, Balogh, Erzsébet, Szabo, Tamás, Olah, Éva
Published in American journal of medical genetics. Part A (01.04.2012)
Published in American journal of medical genetics. Part A (01.04.2012)
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Blepharophimosis mental retardation syndrome Say‐Barber/Biesecker/Young‐Simpson type – New findings with neuroimaging
Szakszon, Katalin, Berényi, Ervin, Jakab, András, Bessenyei, Beáta, Balogh, Erzsébet, Köbling, Tamás, Szilvássy, Judit, Knegt, Alida C., Oláh, Éva
Published in American journal of medical genetics. Part A (01.03.2011)
Published in American journal of medical genetics. Part A (01.03.2011)
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Meiotic segregation study of a novel t(3;6)(q21;q23) in an infertile man using fluorescence in situ hybridization (FISH)
Mokánszki, Attila, Ujfalusi, Anikó, Balogh, Erzsébet, Sümegi, Andrea, Antal-Szalmás, Péter, Bazsáné, Zsuzsa Kassai, Molnár, Zsuzsanna, Varga, Attila, Sápy, Tamás, Jakab, Attila, Oláh, Éva
Published in Systems biology in reproductive medicine (01.06.2012)
Published in Systems biology in reproductive medicine (01.06.2012)
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Endocrine and anatomical findings in a case of Solitary Median Maxillary Central Incisor Syndrome
Szakszon, Katalin, Felszeghy, Enikő, Csízy, István, Józsa, Tamás, Káposzta, Rita, Balogh, Erzsébet, Oláh, Éva, Balogh, István, Berényi, Ervin, Knegt, Alida C, Ilyés, István
Published in European journal of medical genetics (01.02.2012)
Published in European journal of medical genetics (01.02.2012)
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Deletion 15q26 syndrome
Szakszon, Katalin, Ujfalusi, Anikó, Balogh, Erzsébet, Mogyorósy, Gábor, Felszeghy, Enikő, Szilvássy, Judit, Horkay, Edit, Berényi, Ervin, Merő, Gabriella, Knegt, Alida C
Published in Orvosi hetilap (02.03.2014)
Published in Orvosi hetilap (02.03.2014)
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