Knegt AC - Search Results

1

Chromosomal abnormalities and copy number variations in fetal left-sided congenital heart defects.

Jansen FA, Hoffer MJ, van Velzen CL, Plati SK, Rijlaarsdam ME, Clur SA, Blom NA, Pajkrt E, Bhola SL, Knegt AC, de Boer MA, Haak MC. Jansen FA, et al. Among authors: knegt ac. Prenat Diagn. 2016 Feb;36(2):177-85. doi: 10.1002/pd.4767. Epub 2016 Feb 3. Prenat Diagn. 2016. PMID: 26716421

2

The prevalence of genetic diagnoses in fetuses with severe congenital heart defects.

van Nisselrooij AEL, Lugthart MA, Clur SA, Linskens IH, Pajkrt E, Rammeloo LA, Rozendaal L, Blom NA, van Lith JMM, Knegt AC, Hoffer MJV, Aten E, Santen GWE, Haak MC. van Nisselrooij AEL, et al. Among authors: knegt ac. Genet Med. 2020 Jul;22(7):1206-1214. doi: 10.1038/s41436-020-0791-8. Epub 2020 Apr 28. Genet Med. 2020. PMID: 32341573 Free PMC article.

3

Prenatal sonographic features can accurately determine parental origin in triploid pregnancies.

Lugthart MA, Horenblas J, Kleinrouweler EC, Engels M, Knegt AC, Huijsdens K, van Leeuwen E, Pajkrt E. Lugthart MA, et al. Among authors: knegt ac. Prenat Diagn. 2020 May;40(6):705-714. doi: 10.1002/pd.5666. Epub 2020 Mar 3. Prenat Diagn. 2020. PMID: 32039494 Free PMC article.

4

Prenatal diagnosis of a trisomy 7/trisomy 13 mosaicism.

Huijsdens-van Amsterdam K, Barge-Schaapveld DQ, Mathijssen IB, Alders M, Pajkrt E, Knegt AC. Huijsdens-van Amsterdam K, et al. Among authors: knegt ac. Mol Cytogenet. 2012 Jan 27;5(1):8. doi: 10.1186/1755-8166-5-8. Mol Cytogenet. 2012. PMID: 22284936 Free PMC article.

5

Aiming at multidisciplinary consensus: what should be detected in prenatal diagnosis?

Boormans EM, Birnie E, Knegt AC, Schuring-Blom GH, Bonsel GJ, van Lith JM. Boormans EM, et al. Among authors: knegt ac. Prenat Diagn. 2010 Nov;30(11):1049-56. doi: 10.1002/pd.2609. Prenat Diagn. 2010. PMID: 20799375

6

Genetic analysis of fetal nucleated red blood cells from CVS washings.

Jakobs ME, van Lith JM, de Graaf IM, Knegt AC, Hoovers JM. Jakobs ME, et al. Among authors: knegt ac. Prenat Diagn. 2000 Oct;20(10):832-4. Prenat Diagn. 2000. PMID: 11038464

7

Prenatal diagnosis of a karyotypically normal pregnancy in a mother with a supernumerary neocentric 13q21 -->13q22 chromosome and balancing reciprocal deletion.

Knegt AC, Li S, Engelen JJ, Bijlsma EK, Warburton PE. Knegt AC, et al. Prenat Diagn. 2003 Mar;23(3):215-20. doi: 10.1002/pd.559. Prenat Diagn. 2003. PMID: 12627422

8

FISH analysis of fetal nucleated red blood cells from CVS washings in cases of aneuploidy.

Schuring-Blom GH, Hoovers JM, van Lith JM, Knegt AC, Leschot NJ. Schuring-Blom GH, et al. Among authors: knegt ac. Prenat Diagn. 2001 Oct;21(10):864-7. doi: 10.1002/pd.160. Prenat Diagn. 2001. PMID: 11746131

9

Inherited unbalanced structural chromosome abnormalities at prenatal chromosome analysis are rarely ascertained through recurrent miscarriage.

Franssen MT, Korevaar JC, Tjoa WM, Leschot NJ, Bossuyt PM, Knegt AC, Suykerbuyk RF, Hochstenbach R, van der Veen F, Goddijn M. Franssen MT, et al. Among authors: knegt ac. Prenat Diagn. 2008 May;28(5):408-11. doi: 10.1002/pd.1960. Prenat Diagn. 2008. PMID: 18395875

10

[Rapid prenatal diagnosis of chromosomal abnormalities; limitations and possibilities].

Boormans EM, van Lith JM, Bilardo CM, Knegt AC, Oepkes D, Hoffer MJ, Boon EM, Wildschut HI, Galjaard RJ, Schuring-Blom GH, van Oppen AC, Smits A, Creemers J, Go A, Nieuwint A, Nijhuis JG, de Die C, Bonsel GJ, Birnie E, Leschot N. Boormans EM, et al. Among authors: knegt ac. Ned Tijdschr Geneeskd. 2006 Nov 4;150(44):2455; author reply 2455. Ned Tijdschr Geneeskd. 2006. PMID: 17131707 Dutch. No abstract available.

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