Works by Govaerts, L.

Results: 24

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

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

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

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

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

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

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

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

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

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

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

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

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