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Brigitte H W Faas

Showing results (11-20 of 29) with videos related to

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Prenatal Diagnosis|January 17, 2016
Validation of two-channel sequencing-by-synthesis for noninvasive prenatal testing of fetal whole and partial chromosome aberrationsKornelia Neveling, Djie Tjwan Thung, Lean Beulen, et al.
Prenatal Diagnosis|December 13, 2006
Fetal anomaly scan potentially will replace routine AFAFP assays for the detection of neural tube defectsAngelique J A Kooper, Dagmar de Bruijn, Conny M A van Ravenwaaij-Arts, et al.
Clinical Chemistry|December 16, 2016
Combined Count- and Size-Based Analysis of Maternal Plasma DNA for Noninvasive Prenatal Detection of Fetal Subchromosomal Aberrations Facilitates Elucidation of the Fetal and/or Maternal Origin of the AberrationsStephanie C Y Yu, Peiyong Jiang, K C Allen Chan, et al.
Prenatal Diagnosis|October 18, 2008
Multiplex ligation-dependent probe amplification (MLPA) as a stand-alone test for rapid aneuploidy detection in amniotic fluid cellsAngelique J A Kooper, Brigitte H W Faas, Ellen Kater-Baats, et al.
American Journal of Medical Genetics. Part A|September 24, 2025
Clinically Irrelevant Terminal 16q21 Deletion Detected by NIPT Is Attributable to Inherited Fragility at FRA16BServi J C Stevens, Wanwisa van Dijk, Nicole Y Souren, et al.
Ebiomedicine|February 16, 2024
Early detection of active Human CytomegaloVirus (hCMV) infection in pregnant women using data generated for noninvasive fetal aneuploidy testingBrigitte H W Faas, Galuh Astuti, Willem J G Melchers, et al.
The Journal of Molecular Diagnostics : JMD|December 17, 2008
Detection of chromosome aneuploidies in chorionic villus samples by multiplex ligation-dependent probe amplificationAngelique J A Kooper, Brigitte H W Faas, Ton Feuth, et al.
European Journal of Human Genetics : EJHG|January 17, 2013
Prenatal diagnostic testing of the Noonan syndrome genes in fetuses with abnormal ultrasound findingsEllen A Croonen, Willy M Nillesen, Kyra E Stuurman, et al.
Prenatal Diagnosis|May 19, 2025
Clinical Outcome and Risk Factors for Progression of Prenatally Diagnosed Fetal Ventriculomegaly: A Retrospective Multicenter StudyAnouk Moens, Zoe Albersnagel, Marieke B Veenhof, et al.
Clinical Biochemistry|August 13, 2013
Reliable noninvasive prenatal testing by massively parallel sequencing of circulating cell-free DNA from maternal plasma processed up to 24h after venipunctureKaren Buysse, Lean Beulen, Ingrid Gomes, et al.
Pageof 3

Showing results (11-20 of 29) with videos related to

Sort By:
Pageof 3
Prenatal Diagnosis|January 17, 2016
Validation of two-channel sequencing-by-synthesis for noninvasive prenatal testing of fetal whole and partial chromosome aberrationsKornelia Neveling, Djie Tjwan Thung, Lean Beulen, et al.
Prenatal Diagnosis|December 13, 2006
Fetal anomaly scan potentially will replace routine AFAFP assays for the detection of neural tube defectsAngelique J A Kooper, Dagmar de Bruijn, Conny M A van Ravenwaaij-Arts, et al.
Clinical Chemistry|December 16, 2016
Combined Count- and Size-Based Analysis of Maternal Plasma DNA for Noninvasive Prenatal Detection of Fetal Subchromosomal Aberrations Facilitates Elucidation of the Fetal and/or Maternal Origin of the AberrationsStephanie C Y Yu, Peiyong Jiang, K C Allen Chan, et al.
Prenatal Diagnosis|October 18, 2008
Multiplex ligation-dependent probe amplification (MLPA) as a stand-alone test for rapid aneuploidy detection in amniotic fluid cellsAngelique J A Kooper, Brigitte H W Faas, Ellen Kater-Baats, et al.
American Journal of Medical Genetics. Part A|September 24, 2025
Clinically Irrelevant Terminal 16q21 Deletion Detected by NIPT Is Attributable to Inherited Fragility at FRA16BServi J C Stevens, Wanwisa van Dijk, Nicole Y Souren, et al.
Ebiomedicine|February 16, 2024
Early detection of active Human CytomegaloVirus (hCMV) infection in pregnant women using data generated for noninvasive fetal aneuploidy testingBrigitte H W Faas, Galuh Astuti, Willem J G Melchers, et al.
The Journal of Molecular Diagnostics : JMD|December 17, 2008
Detection of chromosome aneuploidies in chorionic villus samples by multiplex ligation-dependent probe amplificationAngelique J A Kooper, Brigitte H W Faas, Ton Feuth, et al.
European Journal of Human Genetics : EJHG|January 17, 2013
Prenatal diagnostic testing of the Noonan syndrome genes in fetuses with abnormal ultrasound findingsEllen A Croonen, Willy M Nillesen, Kyra E Stuurman, et al.
Prenatal Diagnosis|May 19, 2025
Clinical Outcome and Risk Factors for Progression of Prenatally Diagnosed Fetal Ventriculomegaly: A Retrospective Multicenter StudyAnouk Moens, Zoe Albersnagel, Marieke B Veenhof, et al.
Clinical Biochemistry|August 13, 2013
Reliable noninvasive prenatal testing by massively parallel sequencing of circulating cell-free DNA from maternal plasma processed up to 24h after venipunctureKaren Buysse, Lean Beulen, Ingrid Gomes, et al.
Pageof 3