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Page 1
Investigating the role of ASCC1 in the causation of bone fragility.
Front Endocrinol (Lausanne). 2023 Jun 30;14:1137573. doi: 10.3389/fendo.2023.1137573. eCollection 2023.
Front Endocrinol (Lausanne). 2023.
PMID: 37455927
Free PMC article.
Case Report and Review of the Literature: A New and a Recurrent Variant in the VARS2 Gene Are Associated With Isolated Lethal Hypertrophic Cardiomyopathy, Hyperlactatemia, and Pulmonary Hypertension in Early Infancy.
Kušíková K, Feichtinger RG, Csillag B, Kalev OK, Weis S, Duba HC, Mayr JA, Weis D.
Kušíková K, et al. Among authors: csillag b.
Front Pediatr. 2021 Apr 16;9:660076. doi: 10.3389/fped.2021.660076. eCollection 2021.
Front Pediatr. 2021.
PMID: 33937156
Free PMC article.
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Somatic mosaic monosomy 7 and UPD7q in a child with MIRAGE syndrome caused by a novel SAMD9 mutation.
Csillag B, Ilencikova D, Meissl M, Webersinke G, Laccone F, Narumi S, Haas O, Duba HC.
Csillag B, et al.
Pediatr Blood Cancer. 2019 Apr;66(4):e27589. doi: 10.1002/pbc.27589. Epub 2018 Dec 19.
Pediatr Blood Cancer. 2019.
PMID: 30565860
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