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Schwaberger, B, Pichler, G, Urlesberger, B, Hohl, A, Pessenhofer, H, Kohla, B, Köstl, G, Kerbl, R
Published in Archives of disease in childhood (01.10.2012)
Published in Archives of disease in childhood (01.10.2012)
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Molecular cytogenetics and phenotype characterization of a de novo pure partial trisomy 10(q24.33-qter)
Petek, E, Köstl, G, Rauter, L, Mutz, I, Wagner, K, Kroisel, P M
Published in Clinical dysmorphology (01.04.2001)
Published in Clinical dysmorphology (01.04.2001)
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Characterization of a de novo partial trisomy 22q13-qter in a patient by microFISH
Petek, E, Köstl, G, Mutz, I, Wagner, K, Kroisel, P M
Published in Clinical dysmorphology (01.01.2000)
Published in Clinical dysmorphology (01.01.2000)
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Classification of sudden infant death (SID) cases in a multidisciplinary setting. Ten years experience in Styria (Austria)
Kerbl, Reinhold, Zotter, Heinz, Einspieler, Christa, Roll, Peter, Ratschek, Manfred, Köstl, Gerhard, Strenger, Volker, Hoffmann, Erna, Perrogon, Anni, Zötsch, Waltraud, Schober, Peter, Gränz, Alfred, Sauseng, Werner, Bachler, Isolde, Kenner, Thomas, Ipsiroglu, Osman, Kurz, Ronald
Published in Wiener Klinische Wochenschrift (30.12.2003)
Published in Wiener Klinische Wochenschrift (30.12.2003)
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