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Diane Van Opstal

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Expert Review of Molecular Diagnostics|February 12, 2016
Cytogenetic confirmation of a positive NIPT result: evidence-based choice between chorionic villus sampling and amniocentesis depending on chromosome aberrationDiane Van Opstal, Malgorzata I Srebniak
Human Reproduction Update|March 10, 2004
The development of cytogenetically normal, abnormal and mosaic embryos: a theoretical modelFrans J Los, Diane Van Opstal, Cardi van den Berg
Human Mutation|May 16, 2013
0.5 Mb array as a first-line prenatal cytogenetic test in cases without ultrasound abnormalities and its implementation in clinical practiceMalgorzata I Srebniak, Lisanne Mout, Diane Van Opstal, et al.
Prenatal Diagnosis|March 16, 2006
(Potential) false-negative diagnoses in chorionic villi and a review of the literatureCardi van den Berg, Diane Van Opstal, Joke Polak-Knook, et al.
AJP Reports|May 25, 2013
Prenatal diagnosis of alobar holoprosencephaly, cyclopia, proboscis, and isochromosome 18q in the second trimesterMeike Bangma, Simone Lunshof, Diane Van Opstal, et al.
Molecular Cytogenetics|January 18, 2011
Multiplex ligation dependent probe amplification (MLPA) for rapid distinction between unique sequence positive and negative marker chromosomes in prenatal diagnosisDiane Van Opstal, Marjan Boter, Petra Noomen, et al.
European Journal of Human Genetics : EJHG|June 23, 2011
Application of SNP array for rapid prenatal diagnosis: implementation, genetic counselling and diagnostic flowMalgorzata Srebniak, Marjan Boter, Grétel Oudesluijs, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|July 15, 2009
The use of comparative genomic hybridization and fluorescent in situ hybridization in postmortem pathology investigation of congenital malformationsNatascha Goemaere, Hannie Douben, Diane Van Opstal, et al.
The Journal of Clinical Investigation|January 4, 2024
Single-cell DNA sequencing reveals a high incidence of chromosomal abnormalities in human blastocystsEffrosyni A Chavli, Sjoerd J Klaasen, Diane Van Opstal, et al.
Molecular Cytogenetics|January 10, 2021
Patient-friendly integrated first trimester screening by NIPT and fetal anomaly scanMalgorzata Ilona Srebniak, Maarten F C M Knapen, Marieke Joosten, et al.
Pageof 6

Showing results (1-10 of 51) with videos related to

Sort By:
Pageof 6
Expert Review of Molecular Diagnostics|February 12, 2016
Cytogenetic confirmation of a positive NIPT result: evidence-based choice between chorionic villus sampling and amniocentesis depending on chromosome aberrationDiane Van Opstal, Malgorzata I Srebniak
Human Reproduction Update|March 10, 2004
The development of cytogenetically normal, abnormal and mosaic embryos: a theoretical modelFrans J Los, Diane Van Opstal, Cardi van den Berg
Human Mutation|May 16, 2013
0.5 Mb array as a first-line prenatal cytogenetic test in cases without ultrasound abnormalities and its implementation in clinical practiceMalgorzata I Srebniak, Lisanne Mout, Diane Van Opstal, et al.
Prenatal Diagnosis|March 16, 2006
(Potential) false-negative diagnoses in chorionic villi and a review of the literatureCardi van den Berg, Diane Van Opstal, Joke Polak-Knook, et al.
AJP Reports|May 25, 2013
Prenatal diagnosis of alobar holoprosencephaly, cyclopia, proboscis, and isochromosome 18q in the second trimesterMeike Bangma, Simone Lunshof, Diane Van Opstal, et al.
Molecular Cytogenetics|January 18, 2011
Multiplex ligation dependent probe amplification (MLPA) for rapid distinction between unique sequence positive and negative marker chromosomes in prenatal diagnosisDiane Van Opstal, Marjan Boter, Petra Noomen, et al.
European Journal of Human Genetics : EJHG|June 23, 2011
Application of SNP array for rapid prenatal diagnosis: implementation, genetic counselling and diagnostic flowMalgorzata Srebniak, Marjan Boter, Grétel Oudesluijs, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|July 15, 2009
The use of comparative genomic hybridization and fluorescent in situ hybridization in postmortem pathology investigation of congenital malformationsNatascha Goemaere, Hannie Douben, Diane Van Opstal, et al.
The Journal of Clinical Investigation|January 4, 2024
Single-cell DNA sequencing reveals a high incidence of chromosomal abnormalities in human blastocystsEffrosyni A Chavli, Sjoerd J Klaasen, Diane Van Opstal, et al.
Molecular Cytogenetics|January 10, 2021
Patient-friendly integrated first trimester screening by NIPT and fetal anomaly scanMalgorzata Ilona Srebniak, Maarten F C M Knapen, Marieke Joosten, et al.
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