L C P Govaerts - JoVE Visualize

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Prenatal Diagnosis|September 17, 2003

Prenatal detection of complex chromosomal aberrations using advanced molecular cytogenetic techniquesJ M de Pater, L C P Govaerts, S A de Man, et al.

Clinical Genetics|August 20, 2014

Pregnant couples at increased risk for common aneuploidies choose maximal information from invasive genetic testingS L van der Steen, K E M Diderich, S R Riedijk, et al.

Journal of Genetic Counseling|May 26, 2016

The Psychological Impact of Prenatal Diagnosis and Disclosure of Susceptibility Loci: First Impressions of Parents' ExperiencesS L van der Steen, S R Riedijk, J Verhagen-Visser, et al.

American Journal of Medical Genetics. Part A|September 17, 2004

Familial insertion (3;5)(q25.3;q22.1q31.3) with deletion or duplication of chromosome region 5q22.1-5q31.3 in ten unbalanced carriersY H J M Arens, J J M Engelen, L C P Govaerts, et al.

Journal of Genetic Counseling|July 5, 2017

Choosing between Higher and Lower Resolution Microarrays: do Pregnant Women Have Sufficient Knowledge to Make Informed Choices Consistent with their Attitude?S L van der Steen, E M Bunnik, M G Polak, et al.

Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|April 23, 2016

Prenatal and postnatal findings in small-for-gestational-age fetuses without structural ultrasound anomalies at 18-24 weeksM C de Wit, M I Srebniak, M Joosten, et al.

Neurobiology of Disease|February 3, 2007

Contribution of CYLN2 and GTF2IRD1 to neurological and cognitive symptoms in Williams SyndromeJ M van Hagen, J N van der Geest, R S van der Giessen, et al.

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Showing results (11-20 of 17) with videos related to

Sort By:

Pageof 2

You have reached the last page of results.This site can display upto 17 results.

Prenatal Diagnosis|September 17, 2003

Prenatal detection of complex chromosomal aberrations using advanced molecular cytogenetic techniquesJ M de Pater, L C P Govaerts, S A de Man, et al.

Clinical Genetics|August 20, 2014

Pregnant couples at increased risk for common aneuploidies choose maximal information from invasive genetic testingS L van der Steen, K E M Diderich, S R Riedijk, et al.

Journal of Genetic Counseling|May 26, 2016

The Psychological Impact of Prenatal Diagnosis and Disclosure of Susceptibility Loci: First Impressions of Parents' ExperiencesS L van der Steen, S R Riedijk, J Verhagen-Visser, et al.

American Journal of Medical Genetics. Part A|September 17, 2004

Familial insertion (3;5)(q25.3;q22.1q31.3) with deletion or duplication of chromosome region 5q22.1-5q31.3 in ten unbalanced carriersY H J M Arens, J J M Engelen, L C P Govaerts, et al.

Journal of Genetic Counseling|July 5, 2017

Choosing between Higher and Lower Resolution Microarrays: do Pregnant Women Have Sufficient Knowledge to Make Informed Choices Consistent with their Attitude?S L van der Steen, E M Bunnik, M G Polak, et al.

Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|April 23, 2016

Prenatal and postnatal findings in small-for-gestational-age fetuses without structural ultrasound anomalies at 18-24 weeksM C de Wit, M I Srebniak, M Joosten, et al.

Neurobiology of Disease|February 3, 2007

Contribution of CYLN2 and GTF2IRD1 to neurological and cognitive symptoms in Williams SyndromeJ M van Hagen, J N van der Geest, R S van der Giessen, et al.

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