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Autor:
Miltoft, Caroline Borregaard, Rode, Line, Bundgaard, Jens René, Johansen, Peter, Tabor, Ann, Miltoft, Caroline Borregaard, Bundgaard, Jens René
Publikováno v:
Fetal Diagnosis & Therapy; 2020, Vol. 47 Issue 3, p228-236, 9p
Akademický článek
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Autor:
Becher, Naja, Miltoft, Caroline Borregaard, Pedersen, Lars Henning, Vogel, Ida, Petersen, Olav Bjørn
Publikováno v:
Becher, N, Miltoft, C B, Pedersen, L H, Vogel, I & Petersen, O B 2018, Whole Exome Sequencing in Prenatal Diagnostics . DFMS Guideline . < http://www.dfms.dk/images/Guidelines/Exom_rundsendt_100118.pdf >
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::3a05ea540720da21934080b755819acd
https://pure.au.dk/portal/da/publications/whole-exome-sequencing-in-prenatal-diagnostics(b1752178-eeb4-40fc-aea5-e089793459ec).html
https://pure.au.dk/portal/da/publications/whole-exome-sequencing-in-prenatal-diagnostics(b1752178-eeb4-40fc-aea5-e089793459ec).html
Autor:
Miltoft, Caroline Borregaard, Wulff, Camilla B, Kjærgaard, Susanne, Ekelund, Charlotte K., Tabor, Ann, Zingenberg, Helle, Jørgensen, Finn Stener, Shalmi, Anne-Cathrine, Thagaard, Ida Näslund, Skibsted, Lillian, Hessellund, Anette, Sperling, Lene Søndergaard, Mogensen, Helle, Ibsen, Mette, Brendstrup, Lene, Petersen, Olav Bjørn, Jensen, Hanne Søndergaard, Vase, Laura, Østergaard, Marianne, Kamper, Christina H., Sørensen, Anne, Størup, Birgitte
Publikováno v:
Miltoft, C B, Wulff, C B, Kjærgaard, S, Ekelund, C K, Tabor, A, Zingenberg, H, Jørgensen, F S, Shalmi, A-C, Thagaard, I N, Skibsted, L, Hessellund, A, Sperling, L S, Mogensen, H, Ibsen, M, Brendstrup, L, Petersen, O B, Jensen, H S, Vase, L, Østergaard, M, Kamper, C H, Sørensen, A, Størup, B & the Danish Fetal Medicine Study Group 2017, ' Parental Decisions about Prenatal Screening and Diagnosis among Infants with Trisomy 21 in a National Cohort with High Uptake of Combined First-Trimester Screening ', Fetal Diagnosis and Therapy, vol. 41, no. 3, pp. 209-214 . https://doi.org/10.1159/000448093
Introduction: The aim was to investigate the parental decisions about prenatal screening and diagnosis among infants with trisomy 21 (T21) in a national cohort with high uptake of combined first-trimester screening (cFTS). Material and Methods: This
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fd88ff0032bdac9b96c001791fe288fc
https://pure.au.dk/portal/da/publications/parental-decisions-about-prenatal-screening-and-diagnosis-among-infants-with-trisomy-21-in-a-national-cohort-with-high-uptake-of-combined-firsttrimester-screening(e9f8ed91-a94d-43ef-b124-523e28b46d6d).html
https://pure.au.dk/portal/da/publications/parental-decisions-about-prenatal-screening-and-diagnosis-among-infants-with-trisomy-21-in-a-national-cohort-with-high-uptake-of-combined-firsttrimester-screening(e9f8ed91-a94d-43ef-b124-523e28b46d6d).html
Autor:
Miltoft, Caroline Borregaard, Ekelund, Charlotte Kvist, Hansen, Bo Mølholm, Lando, Ane, Tabor, Ann, Petersen, Olav Bjørn, Skovbo, Peter, Jørgensen, Finn Stener, Sperling, Lene, Zingenberg, Helle, Nikkilä, Annamari, Shalmi, Anne Cathrine, Stornes, Inger, Ersbak, Vibeke
Publikováno v:
Miltoft, C B, Ekelund, C K, Hansen, B M, Lando, A, Tabor, A, Petersen, O B, Skovbo, P, Jørgensen, F S, Sperling, L, Zingenberg, H, Nikkilä, A, Shalmi, A C, Stornes, I, Ersbak, V & and the Fetal Medicine Study Group: 2012, ' Increased nuchal translucency, normal karyotype and infant development ', Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology, vol. 39, no. 1, pp. 28-33 . https://doi.org/10.1002/uog.10060
OBJECTIVE: To investigate, if chromosomally normal fetuses with a nuchal translucency (NT) ≥ 99(th) percentile (corresponding to 3.5 mm) in first trimester have an increased risk of delayed development at two years of age. METHODS: The study includ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pure_au_____::54f9e9ff921cee69b391b78a09a9125e
https://pure.au.dk/portal/da/publications/increased-nuchal-translucency-normal-karyotype-and-infant-development(edd4b63e-686d-4583-9a45-59bc2afbf6e6).html
https://pure.au.dk/portal/da/publications/increased-nuchal-translucency-normal-karyotype-and-infant-development(edd4b63e-686d-4583-9a45-59bc2afbf6e6).html
Autor:
Miltoft, Caroline Borregaard, Ekelund, Charlotte Kvist, Hansen, Bo Mølholm, Lando, Ane, Petersen, Olav Bjørn, Skovbo, Peter, Jørgensen, Finn Stener, Sperling, Lene, Zingenberg, Helle, Nikkilä, Annamari, Shalmi, Anne Cathrine, Stornes, Inger, Ersbak, Vibeke, Tabor, Ann
Publikováno v:
Miltoft, C B, Ekelund, C K, Hansen, B M, Lando, A, Petersen, O B, Skovbo, P, Jørgensen, F S, Sperling, L, Zingenberg, H, Nikkilä, A, Shalmi, A C, Stornes, I, Ersbak, V & Tabor, A 2011, ' OC02.03: Increased nuchal translucency, normal karyotype and infant development ', ISUOG World Congress, Los Angeles, United States, 18/09/2011-22/09/2011 . https://doi.org/10.1002/uog.9103
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pure_au_____::e0b7d87f1a45ae2fb286837fc05b459b
https://pure.au.dk/portal/da/publications/oc0203-increased-nuchal-translucency-normal-karyotype-and-infant-development(f3a50b52-d89d-4c75-aa34-1c8cbe54eaaa).html
https://pure.au.dk/portal/da/publications/oc0203-increased-nuchal-translucency-normal-karyotype-and-infant-development(f3a50b52-d89d-4c75-aa34-1c8cbe54eaaa).html
Akademický článek
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