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Placental mosaicism in the era of chromosomal microarrays.
Vogel I, Vestergaard EM, Lildballe DL, Christensen R, Hoseth GE, Petersen AC, Bogaard P, Sørensen AN. Vogel I, et al. Among authors: christensen r. Eur J Med Genet. 2020 Apr;63(4):103778. doi: 10.1016/j.ejmg.2019.103778. Epub 2019 Sep 30. Eur J Med Genet. 2020. PMID: 31580923
Eating behavior, prenatal and postnatal growth in Angelman syndrome.
Mertz LG, Christensen R, Vogel I, Hertz JM, Østergaard JR. Mertz LG, et al. Among authors: christensen r. Res Dev Disabil. 2014 Nov;35(11):2681-90. doi: 10.1016/j.ridd.2014.07.025. Epub 2014 Jul 26. Res Dev Disabil. 2014. PMID: 25064682
Chromosomal microarray in fetuses with increased nuchal translucency.
Lund IC, Christensen R, Petersen OB, Vogel I, Vestergaard EM. Lund IC, et al. Among authors: christensen r. Ultrasound Obstet Gynecol. 2015 Jan;45(1):95-100. doi: 10.1002/uog.14726. Ultrasound Obstet Gynecol. 2015. PMID: 25393210 Free article.
PBX1 haploinsufficiency leads to syndromic congenital anomalies of the kidney and urinary tract (CAKUT) in humans.
Le Tanno P, Breton J, Bidart M, Satre V, Harbuz R, Ray PF, Bosson C, Dieterich K, Jaillard S, Odent S, Poke G, Beddow R, Digilio MC, Novelli A, Bernardini L, Pisanti MA, Mackenroth L, Hackmann K, Vogel I, Christensen R, Fokstuen S, Béna F, Amblard F, Devillard F, Vieville G, Apostolou A, Jouk PS, Guebre-Egziabher F, Sartelet H, Coutton C. Le Tanno P, et al. Among authors: christensen r. J Med Genet. 2017 Jul;54(7):502-510. doi: 10.1136/jmedgenet-2016-104435. Epub 2017 Mar 7. J Med Genet. 2017. PMID: 28270404
1,966 results