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P GOVAERTS

Showing results (71-80 of 84) with videos related to

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Prenatal Diagnosis|July 20, 2019
Placental studies elucidate discrepancies between NIPT showing a structural chromosome aberration and a differently abnormal fetal karyotypeDiane Van Opstal, Stefanie van Veen, Marieke Joosten, 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.
Molecular Cytogenetics|September 10, 2016
Enlarged NT (≥3.5 mm) in the first trimester - not all chromosome aberrations can be detected by NIPTMalgorzata I Srebniak, Merel C de Wit, Karin E M Diderich, et al.
Acta Chirurgica Belgica|March 1, 1983
[Diverticular disease of the left colon. Belgian surgical experience. Multicenter study of 962 cases]P Mendes da Costa, J Ansay, A Beernaerts, 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.
Molecular Genetics & Genomic Medicine|December 3, 2019
Social and medical need for whole genome high resolution NIPTMalgorzata I Srebniak, Maarten F C M Knapen, Lutgarde C P Govaerts, 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.
Prenatal Diagnosis|September 7, 2018
Unexpected finding of uniparental disomy mosaicism in term placentas: Is it a common feature in trisomic placentas?Diane Van Opstal, Karin E M Diderich, Marieke Joosten, et al.
Acta Obstetricia Et Gynecologica Scandinavica|November 29, 2020
The potential diagnostic yield of whole exome sequencing in pregnancies complicated by fetal ultrasound anomaliesKarin E M Diderich, Kathleen Romijn, Marieke Joosten, et al.
Human Mutation|April 15, 2017
The influence of SNP-based chromosomal microarray and NIPT on the diagnostic yield in 10,000 fetuses with and without fetal ultrasound anomaliesMalgorzata I Srebniak, Maarten F C M Knapen, Marike Polak, et al.
Pageof 9

Showing results (71-80 of 84) with videos related to

Sort By:
Pageof 9
Prenatal Diagnosis|July 20, 2019
Placental studies elucidate discrepancies between NIPT showing a structural chromosome aberration and a differently abnormal fetal karyotypeDiane Van Opstal, Stefanie van Veen, Marieke Joosten, 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.
Molecular Cytogenetics|September 10, 2016
Enlarged NT (≥3.5 mm) in the first trimester - not all chromosome aberrations can be detected by NIPTMalgorzata I Srebniak, Merel C de Wit, Karin E M Diderich, et al.
Acta Chirurgica Belgica|March 1, 1983
[Diverticular disease of the left colon. Belgian surgical experience. Multicenter study of 962 cases]P Mendes da Costa, J Ansay, A Beernaerts, 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.
Molecular Genetics & Genomic Medicine|December 3, 2019
Social and medical need for whole genome high resolution NIPTMalgorzata I Srebniak, Maarten F C M Knapen, Lutgarde C P Govaerts, 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.
Prenatal Diagnosis|September 7, 2018
Unexpected finding of uniparental disomy mosaicism in term placentas: Is it a common feature in trisomic placentas?Diane Van Opstal, Karin E M Diderich, Marieke Joosten, et al.
Acta Obstetricia Et Gynecologica Scandinavica|November 29, 2020
The potential diagnostic yield of whole exome sequencing in pregnancies complicated by fetal ultrasound anomaliesKarin E M Diderich, Kathleen Romijn, Marieke Joosten, et al.
Human Mutation|April 15, 2017
The influence of SNP-based chromosomal microarray and NIPT on the diagnostic yield in 10,000 fetuses with and without fetal ultrasound anomaliesMalgorzata I Srebniak, Maarten F C M Knapen, Marike Polak, et al.
Pageof 9