Reply: The missing role of diagnosis of confined placental mosaicism in the management of fetal growth restriction

por Eggenhuizen, Geerke M, Go, Attie, Galjaard, Robert Jan
Publicado 2021

Why NIPT should be publicly funded

por Bunnik, Eline Maria, Kater-Kuipers, Adriana, Galjaard, Robert-Jan H, de Beaufort, Inez
Publicado 2020

Should pregnant women be charged for non-invasive prenatal screening? Implications for reproductive autonomy and equal access

por Bunnik, Eline M, Kater-Kuipers, Adriana, Galjaard, Robert-Jan H, de Beaufort, Inez D
Publicado 2020

Rethinking counselling in prenatal screening: An ethical analysis of informed consent in the context of non‐invasive prenatal testing (NIPT)

por Kater‐Kuipers, Adriana, de Beaufort, Inez D., Galjaard, Robert‐Jan H., Bunnik, Eline M.
Publicado 2020

Multiplex ligation dependent probe amplification (MLPA) for rapid distinction between unique sequence positive and negative marker chromosomes in prenatal diagnosis

por Van Opstal, Diane, Boter, Marjan, Noomen, Petra, Srebniak, Malgorzata, Hamers, Guus, Galjaard, Robert-Jan H
Publicado 2011

Confined placental mosaicism and the association with pregnancy outcome and fetal growth: a review of the literature

por Eggenhuizen, Geerke M, Go, Attie, Koster, Maria P H, Baart, Esther B, Galjaard, Robert Jan
Publicado 2021

Variable expression of subclinical phenotypes instead of reduced penetrance in families with mild triphalangeal thumb phenotypes

por Potuijt, Jacob W P, Hoogeboom, Jeannette, de Graaff, Esther, van Nieuwenhoven, Christianne A, Galjaard, Robert Jan H
Publicado 2020

Non‐invasive prenatal test uptake in socioeconomically disadvantaged neighborhoods

por van der Meij, Karuna R. M., Kooij, Caroline, Bekker, Mireille N., Galjaard, Robert‐Jan H., Henneman, Lidewij
Publicado 2021

Is it feasible to select fetuses for prenatal WES based on the prenatal phenotype?

por Diderich, Karin, Joosten, Marieke, Govaerts, Lutgarde, Van Opstal, Diane, Go, Attie, Knapen, Maarten, Galjaard, Robert‐Jan, Hoefsloot, Lies, Srebniak, Malgorzata
Publicado 2019

Prenatally diagnosed submicroscopic familial aberrations at 18p11.32 without phenotypic effect

por Srebniak, Malgorzata I, Boter, Marjan, Verboven-Peerden, Carla MA, Looye-Bruinsma, Gerda AG, Oudesluijs, Gretel, Galjaard, Robert-Jan H, Van Opstal, Diane
Publicado 2011

Intrafamilial variability of the triphalangeal thumb phenotype in a Dutch population: Evidence for phenotypic progression over generations?

por Baas, Martijn, Potuijt, Jacob W.P., Hovius, Steven E.R., Hoogeboom, A. Jeannette M., Galjaard, Robert‐Jan H., van Nieuwenhoven, Christianne A.
Publicado 2017

Variant type and position predict two distinct limb phenotypes in patients with GLI3-mediated polydactyly syndromes

por Baas, Martijn, Burger, Elise Bette, van den Ouweland, Ans MW, Hovius, Steven ER, de Klein, Annelies, van Nieuwenhoven, Christianne A, Galjaard, Robert Jan H
Publicado 2021

Nationwide implementation of the non-invasive prenatal test: Evaluation of a blended learning program for counselors

por Martin, Linda, Gitsels-van der Wal, Janneke T., Bax, Caroline J., Pieters, Mijntje J., Reijerink-Verheij, Jacqueline C. I. Y., Galjaard, Robert-Jan, Henneman, Lidewij
Publicado 2022

A multidisciplinary review of triphalangeal thumb

por Potuijt, Jacob W. P., Galjaard, Robert-Jan H., van der Spek, Peter J., van Nieuwenhoven, Christianne A., Ahituv, Nadav, Oberg, Kerby C., Hovius, Steven E. R.
Publicado 2018

Implementing non‐invasive prenatal testing (NIPT) in the Netherlands: An interview study exploring opinions about and experiences with societal pressure, reimbursement, and an expa...

por Bakkeren, Iris M., Kater‐Kuipers, Adriana, Bunnik, Eline M., Go, Attie T. J. I., Tibben, Aad, de Beaufort, Inez D., Galjaard, Robert‐Jan H., Riedijk, Sam R.
Publicado 2019

Informed choice and routinization of the second-trimester anomaly scan: a national cohort study in the Netherlands

por Lust, Eline E.R., Bronsgeest, Kim, Henneman, Lidewij, Crombag, Neeltje, Bilardo, Caterina M., van Vliet-Lachotzki, Elsbeth H., Galjaard, Robert-Jan H., Sikkel, Esther, Haak, Monique C., Bekker, Mireille N.
Publicado 2023

Economic evaluation of multiplex ligation-dependent probe amplification and karyotyping in prenatal diagnosis: a cost-minimization analysis

por Boormans, Elisabeth M. A., Birnie, Erwin, Hoffer, Mariëtte J. V., Macville, Merryn V. E., Galjaard, Robert-Jan, Schuring-Blom, Gijsbertha H., Bhola, Shama L., Huijsdens, Karin, Smits, Arie, van Lith, Jan M. M.
Publicado 2011

The Psychological Challenges of Replacing Conventional Karyotyping with Genomic SNP Array Analysis in Prenatal Testing

por Riedijk, Sam, Diderich, Karin E. M., van der Steen, Sanne L., Govaerts, Lutgarde C. P., Joosten, Marieke, Knapen, Maarten F. C. M., de Vries, Femke A. T., van Opstal, Diane, Tibben, Aad, Galjaard, Robert-Jan H.
Publicado 2014

Genomic SNP array as a gold standard for prenatal diagnosis of foetal ultrasound abnormalities

por Srebniak, Malgorzata I, Boter, Marjan, Oudesluijs, Gretel O, Cohen-Overbeek, Titia, Govaerts, Lutgarde CP, Diderich, Karin EM, Oegema, Renske, Knapen, Maarten FCM, van de Laar, Ingrid MBH, Joosten, Marieke, Van Opstal, Diane, Galjaard, Robert-Jan H
Publicado 2012

Stable X Chromosome Reactivation in Female Human Induced Pluripotent Stem Cells

por Barakat, Tahsin Stefan, Ghazvini, Mehrnaz, de Hoon, Bas, Li, Tracy, Eussen, Bert, Douben, Hannie, van der Linden, Reinier, van der Stap, Nathalie, Boter, Marjan, Laven, Joop S., Galjaard, Robert-Jan, Grootegoed, J. Anton, de Klein, Annelies, Gribnau, Joost
Publicado 2015