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1972 2
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1990 1
1996 1
2008 1
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2012 1
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2015 5
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20 results

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Page 1
ECEL1 mutation causes fetal arthrogryposis multiplex congenita.
Dohrn N, Le VQ, Petersen A, Skovbo P, Pedersen IS, Ernst A, Krarup H, Petersen MB. Dohrn N, et al. Among authors: skovbo p. Am J Med Genet A. 2015 Apr;167A(4):731-43. doi: 10.1002/ajmg.a.37018. Epub 2015 Feb 23. Am J Med Genet A. 2015. PMID: 25708584
[Diuretics and hypokalemia].
Skovbo P, Bjerregaard P, Hvidt R, Jesting E, Lorentzen F, Hvidt S. Skovbo P, et al. Ugeskr Laeger. 1972 May 15;134(20):1043-7. Ugeskr Laeger. 1972. PMID: 5064948 Danish. No abstract available.
Increased nuchal translucency, normal karyotype and infant development.
Miltoft CB, Ekelund CK, Hansen BM, Lando A, Petersen OB, Skovbo P, Jørgensen FS, Sperling L, Zingenberg H, Nikkila A, Shalmi AC, Stornes I, Ersbak V, Tabor A. Miltoft CB, et al. Among authors: skovbo p. Ultrasound Obstet Gynecol. 2012 Jan;39(1):28-33. doi: 10.1002/uog.10060. Ultrasound Obstet Gynecol. 2012. PMID: 21837765 Free article.
[Down's syndrome risk assessment in Denmark--secondary publication].
Ekelund CK, Andersen HJ, Christensen J, Ersbak V, Farlie R, Henriques C, Holmskov A, Jensen LN, Jørgensen FS, Hessellund A, Larsen T, Olesen AW, Pedersen OB, Poulsen H, Ramb J, Skibsted L, Skovbo P, Sommer S, Sperling L, Sundberg K, Juul SV, Zingenberg H, Tabor A. Ekelund CK, et al. Among authors: skovbo p. Ugeskr Laeger. 2010 Jun 7;172(23):1759-61. Ugeskr Laeger. 2010. PMID: 20552746 Danish.
20 results