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The clinical and molecular spectrum of QRICH1 associated neurodevelopmental disorder.
Hum Mutat. 2022 Feb;43(2):266-282. doi: 10.1002/humu.24308. Epub 2021 Dec 11.
Hum Mutat. 2022.
PMID: 34859529
Free article.
Interstitial deletion of 14q24.3-q32.2 in a male patient with plagiocephaly, BPES features, developmental delay, and congenital heart defects.
Cingöz S, Bache I, Bjerglund L, Ropers HH, Tommerup N, Jensen H, Brøndum-Nielsen K, Tümer Z.
Cingöz S, et al. Among authors: bjerglund l.
Am J Med Genet A. 2011 Jan;155A(1):203-6. doi: 10.1002/ajmg.a.33766.
Am J Med Genet A. 2011.
PMID: 21204233
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Fetal ventriculomegaly due to familial submicroscopic terminal 6q deletions.
Wadt K, Jensen LN, Bjerglund L, Lundstrøm M, Kirchhoff M, Kjaergaard S.
Wadt K, et al. Among authors: bjerglund l.
Prenat Diagn. 2012 Dec;32(12):1212-7. doi: 10.1002/pd.3981. Epub 2012 Oct 14.
Prenat Diagn. 2012.
PMID: 23065819
Review.
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[Fatal pneumonia with Panton Valentine leucocidin-producing Staphylococcus aureus].
Rabøl PH, Dessau RB, Warnecke M, Bjerglund L.
Rabøl PH, et al. Among authors: bjerglund l.
Ugeskr Laeger. 2010 Apr 19;172(16):1190-1.
Ugeskr Laeger. 2010.
PMID: 20423659
Danish.
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