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/vufind/Search/Results?lookfor=%22Becher%2C+Naja%22&type=Person&sort=year
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PubPharm (53)
1
Use of cell-free non-invasive prenatal testing in pregnancies affected by placental mosaicism
enthalten in:
Prenatal diagnosis
| 2024
von
Lund, I.
|
Becher, N.
|
Lildballe, D.
| +4
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2
A decade of change - lessons learned from prenatal diagnostics in Central Denmark region in 2008-2018
enthalten in:
Acta obstetricia et gynecologica Scandinavica
| 2023
von
Lildballe, D.
|
Becher, N.
|
Vestergaard, E.
| +7
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3
How does cell-based non-invasive prenatal test (NIPT) perform against chorionic villus sampling and cell-free NIPT in detecting trisomies and copy number variations? A clinical study from Denmark
enthalten in:
Prenatal diagnosis
| 2023
von
Hatt, L.
|
Ravn, K.
|
Dahl Jeppesen, L.
| +18
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4
A decade of change – lessons learned from prenatal diagnostics in Central Denmark region in 2008–2018
enthalten in:
Acta Obstetricia et Gynecologica Scandinavica
| 2023
von
Lildballe, D.
|
Becher, N.
|
Vestergaard, E.
| +7
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5
Incidental finding of maternal malignancy in an unusual non-invasive prenatal test and a review of similar cases
enthalten in:
Clinical case reports
| 2022
von
Moellgaard, M.
|
Lund, I.
|
Becher, N.
| +4
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6
A novel nonsense variant in MED12 associated with malformations in a female fetus
enthalten in:
Clinical case reports
| 2021
von
Faergeman, S.
|
Becher, N.
|
Andreasen, L.
| +3
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7
Phenotypic heterogeneity and mosaicism in Xia-Gibbs syndrome : Five Danish patients with novel variants in AHDC1
enthalten in:
European journal of medical genetics
| 2021
von
Faergeman, S.
|
Bojesen, A.
|
Rasmussen, M.
| +14
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8
National data on the early clinical use of non-invasive prenatal testing in public and private healthcare in Denmark 2013-2017
enthalten in:
Acta obstetricia et gynecologica Scandinavica
| 2021
von
Lund, I.
|
Petersen, O.
|
Becher, N.
| +14
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9
A novel homozygous variant in C1QBP causes severe IUGR, edema, and cardiomyopathy in two fetuses
enthalten in:
JIMD reports
| 2021
von
Alstrup, M.
|
Vogel, I.
|
Sandager, P.
| +3
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10
Mosaicism for copy number variations in the placenta is even more difficult to interpret than mosaicism for whole chromosome aneuploidy
enthalten in:
Prenatal diagnosis
| 2021
von
Lund, I.
|
Becher, N.
|
Graakjaer, J.
| +6
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Acta obstetricia et gynecologica Scandinavica
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Research Support, Non-U.S. Gov't
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EC 3.4.24.-
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prenatal diagnosis
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Neutrophil Leukocyte
3
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EC 3.4.24.79
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Gynecology and obstetrics
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Intrauterine Infection
2
Matrix Metalloproteinase 8
2
PAPPA protein, human
2
Pregnancy-Associated Plasma Protein-A
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