Search

Author/Creator Hochstenbach, Ron

1. Cell‐free fetal DNA in the maternal circulation originates from the cytotrophoblast: proof from an unique case. Issue 6 (29th April 2015)

Authors:
Hochstenbach, Ron; Nikkels, Peter G. J.; Elferink, Martin G.; Oudijk, Martijn A.; van Oppen, Carla; van Zon, Patrick; van Harssel, Jeske; Schuring‐Blom, Heleen; Page‐Christiaens, Godelieve C. M. L.
Journal:
Clinical case reports
Issue:
Volume 3:Issue 6(2015:Dec.)
Page Start:
489
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

2. De Novo Trisomy 1q10q23.3 Mosaicism Causes Microcephaly, Severe Developmental Delay, and Facial Dysmorphic Features but No Cardiac Anomalies. (31st January 2016)

Authors:
Lo-A-Njoe, Shirley; van der Veken, Lars T.; Vermont, Clementien; Rafael-Croes, Louise; Keizer, Vincent; Hochstenbach, Ron; Knoers, Nine; van Haelst, Mieke M.
Other Names:
Cotter Philip D. Academic Editor.
Journal:
Case reports in genetics
Issue:
Volume 2016(2016)
Page Start:
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

3. Discordant NIPT result in a viable trisomy‐21 pregnancy due to prolonged contribution to cfDNA by a demised trisomy‐14 cotwin. Issue 5 (7th March 2018)

Authors:
Hochstenbach, Ron; Elferink, Martin G.; van Zon, Patrick H. A.; Lichtenbelt, Klaske D.; van Harssel, Jeske; Schuring‐Blom, Heleen; Page‐Christiaens, Godelieve C.M.L.
Journal:
Clinical case reports
Issue:
Volume 6:Issue 5(2018)
Page Start:
788
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

4. Genetic variants in the KDM6B gene are associated with neurodevelopmental delays and dysmorphic features. Issue 7 (23rd May 2019)

Authors:
Stolerman, Elliot S.; Francisco, Elizabeth; Stallworth, Jennifer L.; Jones, Julie R.; Monaghan, Kristin G.; Keller‐Ramey, Jennifer; Person, Richard; Wentzensen, Ingrid M.; McWalter, Kirsty; Keren, Boris; Heron, Benedicte; Nava, Caroline; Heron, Delphine; Kim, Katherine; Burton, Barbara; Al‐Musafr...
Journal:
American journal of medical genetics
Issue:
Volume 179:Issue 7(2019)
Page Start:
1276
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

5. Molecular dissection of germline chromothripsis in a developmental context using patient-derived iPS cells. Issue 1 (December 2017)

Authors:
Middelkamp, Sjors; van Heesch, Sebastiaan; Braat, A.; de Ligt, Joep; van Iterson, Maarten; Simonis, Marieke; van Roosmalen, Markus; Kelder, Martijn; Kruisselbrink, Evelien; Hochstenbach, Ron; Verbeek, Nienke; Ippel, Elly; Adolfs, Youri; Pasterkamp, R.; Kloosterman, Wigard; Kuijk, Ewart; Cuppen, E...
Journal:
Genome medicine
Issue:
Volume 9:Issue 1(2017)
Page Start:
1
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

6. Selective chromosome analysis in couples with two or more miscarriages: case-control study. Issue 7509 (28th June 2005)

Authors:
Franssen, Maureen T M; Korevaar, Johanna C; Leschot, Nico J; Bossuyt, Patrick M M; Knegt, Alida C; Gerssen-Schoorl, Klasien B J; Wouters, Cokkie H; Hansson, Kerstin B M; Hochstenbach, Ron; Madan, Kamlesh; van der Veen, Fulco; Goddijn, Mariette
Journal:
BMJ
Issue:
Volume 331:Issue 7509(2005)
Page Start:
137
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗