Works by Govaerts, L.

Results: 24

Visual depth processing in Williams–Beuren syndrome.
Published in:
Experimental Brain Research, 2005, v. 166, n. 2, p. 200, doi. 10.1007/s00221-005-2355-1
By:
- Van der Geest, J. N.;
- Lagers-van Haselen, G. C.;
- van Hagen, J. M.;
- Brenner, E.;
- Govaerts, L. C. P.;
- de Coo, I. F. M.;
- Frens, M. A.
Publication type:
Article
P16.05: The influence of chromosomal microarray and NIPT on the diagnostic yield in 6,811 high-risk pregnancies without ultrasound anomalies.
Published in:
Ultrasound in Obstetrics & Gynecology, 2017, v. 50, p. 206, doi. 10.1002/uog.18159
By:
- Srebniak, M.I.;
- Knapen, M.;
- Polak, M.;
- Joosten, M.;
- Diderich, K.E.;
- Govaerts, L.;
- Ijcken, W.F.;
- Heydanus, R.;
- Dijkman, A.;
- Toolenaar, T.;
- de Vries, F.A.;
- Knijnenburg, J.;
- Go, A.;
- Galjaard, R.J.;
- Van Opstal, D.
Publication type:
Article
EP06.03: Be aware of a diagnostic delay: Rotterdam's experience with NIPT in 1071 high-risk pregnancies.
Published in:
Ultrasound in Obstetrics & Gynecology, 2017, v. 50, p. 284, doi. 10.1002/uog.18407
By:
- Diderich, K.E.;
- Srebniak, M.I.;
- Knapen, M.;
- Joosten, M.;
- Govaerts, L.;
- Ijcken, W.F.;
- Go, A.;
- Galjaard, R.J.;
- Van Opstal, D.
Publication type:
Article
Prenatal and postnatal findings in small-for-gestational-age fetuses without structural ultrasound anomalies at 18-24 weeks.
Published in:
2017
By:
- de Wit, M. C.;
- Srebniak, M. I.;
- Joosten, M.;
- Govaerts, L. C. P.;
- Kornelisse, R. F.;
- Papatsonis, D. N. M.;
- de Graaff, K.;
- Knapen, M. F. C. M.;
- Bruggenwirth, H. T.;
- de Vries, F. A. T.;
- Van Veen, S.;
- Van Opstal, D.;
- Galjaard, R. J. H.;
- Go, A. T. J. I.
Publication type:
journal article
Whole-genome array as a first-line cytogenetic test in prenatal diagnosis.
Published in:
Ultrasound in Obstetrics & Gynecology, 2015, v. 45, n. 4, p. 363, doi. 10.1002/uog.14745
By:
- Srebniak, M. I.;
- Van Opstal, D.;
- Joosten, M.;
- Diderich, K. E. M.;
- de Vries, F. A. T.;
- Riedijk, S.;
- Knapen, M. F. C. M.;
- Go, A. T. J. I.;
- Govaerts, L. C. P.;
- Galjaard, R.‐J. H.
Publication type:
Article
P13.04: Does genomic microarray add prognostic information in case of the second trimester small-for-gestational age, but structurally normal fetus?
Published in:
Ultrasound in Obstetrics & Gynecology, 2014, v. 44, p. 254, doi. 10.1002/uog.14234
By:
- De Wit, M.C.;
- Srebniak, M.I.;
- Govaerts, L.;
- Joosten, M.S.;
- Knapen, M.;
- Galjaard, R.J.;
- Go, A.
Publication type:
Article
OP35.10: What do pregnant couples want? The preferences of pregnant couples at increased risk for Down's syndrome who are offered a choice in prenatal diagnosis between the clinical outcomes of 5 Mb and 0,5 Mb whole genome SNP array analysis.
Published in:
Ultrasound in Obstetrics & Gynecology, 2014, v. 44, p. 148, doi. 10.1002/uog.13984
By:
- Knapen, M.;
- van der Steen, S.L.;
- Riedijk, S.;
- Diderich, K.;
- Joosten, M.S.;
- Govaerts, L.;
- Opstal, D.V.;
- Galjaard, R.J.;
- Visser, J.;
- Srebniak, M.I.;
- Tibben, A.
Publication type:
Article
Additional value of prenatal genomic array testing in fetuses with isolated structural ultrasound abnormalities and a normal karyotype: a systematic review of the literature.
Published in:
Ultrasound in Obstetrics & Gynecology, 2014, v. 43, n. 2, p. 139, doi. 10.1002/uog.12575
By:
- de wit, M. C.;
- Srebniak, M. I.;
- Govaerts, L. C. P.;
- Van Opstal, D.;
- Galjaard, R. J. H.;
- Go, A. T. J. I.
Publication type:
Article
P05.02: Prenatal ultrasound diagnosis of MYH7 noncompaction cardiomyopathy.
Published in:
Ultrasound in Obstetrics & Gynecology, 2011, v. 38, p. 181, doi. 10.1002/uog.9659
By:
- Cohen-Overbeek, T.;
- Hoedemaekers, Y. M.;
- Schoonderwaldt, E. M.;
- Frohn-Mulder, I. M.;
- Dalinghaus, M.;
- Govaerts, L.;
- Caliskan, K.;
- Dooijes, D.;
- Majoor-Krakauer, D.
Publication type:
Article
Prenatal detection of complex chromosomal aberrations using advanced molecular cytogenetic techniques.
Published in:
Prenatal Diagnosis, 2003, v. 23, n. 9, p. 747, doi. 10.1002/pd.653
By:
- J. M. de Pater;
- L. C. P. Govaerts;
- S. A. de Man;
- C. J. M. van der Sijs-Bos;
- G. C. M. L. Christiaens;
- W. M. van Dam;
- W. H. Loneus;
- J. J. M. Engelen
Publication type:
Article
Monosomy X and omphalocele.
Published in:
1997
By:
- Govaerts, L C;
- Bongers, M Y;
- Lammens, M M;
- Tuerlings, J H;
- van de Kaa, C A
Publication type:
Case Study
Abnormal karyotype in the chorion, not confirmed in a subsequently aborted fetus.
Published in:
1986
By:
- Breed, A.;
- Mantingh, A.;
- Govaerts, L.;
- Boogert, A.;
- Anders, G.;
- Laurini, R.
Publication type:
journal article
Savings and extinction of conditioned eyeblink responses in fragile X syndrome.
Published in:
Genes, Brain & Behavior, 2008, v. 7, n. 7, p. 770, doi. 10.1111/j.1601-183X.2008.00417.x
By:
- Smit, A. E.;
- van der Geest, J. N.;
- Vellema, M.;
- Koekkoek, K. E.;
- Willemsen, R.;
- Govaerts, L. C. P.;
- Oostra, B. A.;
- De Zeeuw, C. I.;
- VanderWerf, F.
Publication type:
Article
Omphalocele: comparison of outcome following prenatal or postnatal diagnosis.
Published in:
Ultrasound in Obstetrics & Gynecology, 2010, v. 36, n. 6, p. 687, doi. 10.1002/uog.7698
By:
- Cohen-Overbeek, T. E.;
- Tong, W. H.;
- Hatzmann, T. R.;
- Wilms, J. F.;
- Govaerts, L. C. P.;
- Galjaaard, R. J. H.;
- Steegers, E. A. P.;
- Hops, W. C. J.;
- Wladimiroff, J. W.;
- Tibboel, D.
Publication type:
Article
P12.16: Omphalocele; comparison of perinatal outcome following a prenatal diagnosis or a diagnosis at birth.
Published in:
Ultrasound in Obstetrics & Gynecology, 2009, v. 34, n. S1, p. 228, doi. 10.1002/uog.7186
By:
- Cohen-Overbeek, T. E.;
- Tong, W. H.;
- Hatzmann, T. R.;
- Wilms, J. F.;
- Govaerts, L. C.;
- Steegers, E. A.;
- Hop, W. C.;
- Wladimiroff, J. W.;
- Tibboel, D.
Publication type:
Article
Exceptional good cognitive and phenotypic profile in a male carrying a mosaic mutation in the FMR1 gene.
Published in:
Clinical Genetics, 2007, v. 72, n. 2, p. 138, doi. 10.1111/j.1399-0004.2007.00829.x
By:
- Govaerts, L. C. P.;
- Smit, A. E.;
- Saris, J. J.;
- VanderWerf, F.;
- Willemsen, R.;
- Bakker, C. E.;
- De Zeeuw, C. I.;
- Oostra, B. A.
Publication type:
Article
Facial and pituitary morphology are related in Dutch patients with GH deficiency.
Published in:
Clinical Endocrinology, 2008, v. 69, n. 1, p. 112, doi. 10.1111/j.1365-2265.2007.03167.x
By:
- de Graaff, L. C. G.;
- Baan, J.;
- Govaerts, L. C. P.;
- Hokken-Koelega, A. C. S.
Publication type:
Article
Choosing between Higher and Lower Resolution Microarrays: do Pregnant Women Have Sufficient Knowledge to Make Informed Choices Consistent with their Attitude?
Published in:
Journal of Genetic Counseling, 2018, v. 27, n. 1, p. 85, doi. 10.1007/s10897-017-0124-5
By:
- van der Steen, S. L.;
- Bunnik, E. M.;
- Polak, M. G.;
- Diderich, K. E. M.;
- Verhagen-Visser, J.;
- Govaerts, L. C. P.;
- Joosten, M.;
- Knapen, M. F. C. M.;
- Go, A. T. J. I.;
- Van Opstal, D.;
- Srebniak, M. I.;
- Galjaard, R. J. H.;
- Tibben, A.;
- Riedijk, S. R.
Publication type:
Article
The Psychological Impact of Prenatal Diagnosis and Disclosure of Susceptibility Loci: First Impressions of Parents' Experiences.
Published in:
Journal of Genetic Counseling, 2016, v. 25, n. 6, p. 1227, doi. 10.1007/s10897-016-9960-y
By:
- Steen, S.;
- Riedijk, S.;
- Verhagen-Visser, J.;
- Govaerts, L.;
- Srebniak, M.;
- Opstal, D.;
- Joosten, M.;
- Knapen, M.;
- Tibben, A.;
- Diderich, K.;
- Galjaard, R.
Publication type:
Article
Outcome of pregnancies complicated by oligohydramnios or anhydramnios of renal origin.
Published in:
Prenatal Diagnosis, 2011, v. 31, n. 11, p. 1039, doi. 10.1002/pd.2827
By:
- Grijseels, E. W. M.;
- van-Hornstra, PTM Echteld;
- Govaerts, L. C. P.;
- Cohen-Overbeek, T. E.;
- de Krijger, R. R.;
- Smit, B. J.;
- Cransberg, K.
Publication type:
Article
An incomplete trisomy 3 rescue resulting in a marker chromosome and UPD(3)--difficulties in interpretation.
Published in:
2008
By:
- Srebniak M;
- Noomen P;
- dos Santos P;
- Halley D;
- van de Graaf R;
- Govaerts L;
- Wouters C;
- Galjaard RJ;
- Van Opstal D
Publication type:
Journal Article
Acute intramural haematoma of the ascending aorta.
Published in:
European Journal of Nuclear Medicine & Molecular Imaging, 2012, v. 39, n. 8, p. 1368, doi. 10.1007/s00259-012-2130-z
By:
- Govaerts, L.;
- Withofs, N.;
- Durieux, R.;
- Spote, V.;
- Hustinx, R.
Publication type:
Article
A genome-wide linkage scan in a Dutch family identifies a premature ovarian failure susceptibility locus.
Published in:
Human Reproduction, 2008, v. 23, n. 12, p. 2835, doi. 10.1093/humrep/den278
By:
- R.A. Oldenburg;
- M.F. van Dooren;
- B. de Graaf;
- E. Simons;
- L. Govaerts;
- S. Swagemakers;
- J.M.H. Verkerk;
- B.A. Oostra;
- A.M. Bertoli-Avella
Publication type:
Article
Genetic risk factors in infertile men with severe oligozoospermia and azoospermia.
Published in:
2002
By:
- Dohle, G. R.;
- Halley, D. J. J.;
- Van Hemel, J. O.;
- Van den Ouweland, A. M. W.;
- Pieters, M. H. E. C.;
- Weber, R. F. A.;
- Govaerts, L. C. P.;
- van den Ouwel, A M W
Publication type:
journal article