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Page 1
Severe Deoxyguanosine Kinase Deficiency in Austria: A 6-Patient Series.
J Pediatr Gastroenterol Nutr. 2019 Jan;68(1):e1-e6. doi: 10.1097/MPG.0000000000002149.
J Pediatr Gastroenterol Nutr. 2019.
PMID: 30589726
Weight and body mass index (BMI): current data for Austrian boys and girls aged 4 to under 19 years.
Mayer M, Gleiss A, Häusler G, Borkenstein M, Kapelari K, Köstl G, Lassi M, Schemper M, Schmitt K, Blümel P.
Mayer M, et al. Among authors: kostl g.
Ann Hum Biol. 2015 Jan;42(1):45-55. doi: 10.3109/03014460.2014.907444. Epub 2014 Apr 24.
Ann Hum Biol. 2015.
PMID: 24761986
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Spontaneous growth in growth hormone deficiency from birth until 7 years of age: development of disease-specific growth curves.
Mayer M, Schmitt K, Kapelari K, Frisch H, Köstl G, Voigt M.
Mayer M, et al. Among authors: kostl g.
Horm Res Paediatr. 2010;74(2):136-44. doi: 10.1159/000281020. Epub 2010 Apr 29.
Horm Res Paediatr. 2010.
PMID: 20424417
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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 PM.
Petek E, et al. Among authors: kostl g.
Clin Dysmorphol. 2001 Apr;10(2):151-3. doi: 10.1097/00019605-200104000-00015.
Clin Dysmorphol. 2001.
PMID: 11310998
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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 PM.
Petek E, et al. Among authors: kostl g.
Clin Dysmorphol. 2000 Jan;9(1):55-7. doi: 10.1097/00019605-200009010-00011.
Clin Dysmorphol. 2000.
PMID: 10649799
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Classification of sudden infant death (SID) cases in a multidisciplinary setting. Ten years experience in Styria (Austria).
Kerbl R, Zotter H, Einspieler C, Roll P, Ratschek M, Köstl G, Strenger V, Hoffmann E, Perrogon A, Zötsch W, Schober P, Gränz A, Sauseng W, Bachler I, Kenner T, Ipsiroglu O, Kurz R; Styrian Sudden Infant Death Study Group.
Kerbl R, et al. Among authors: kostl g.
Wien Klin Wochenschr. 2003 Dec 30;115(24):887-93. doi: 10.1007/BF03040411.
Wien Klin Wochenschr. 2003.
PMID: 14768536
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