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Author/Creator Vermeesch, Joris R.

1. A comprehensive clinical and genetic study in 127 patients with ID in Kinshasa, DR Congo. Issue 9 (8th August 2018)

Authors:
Lumaka, Aimé; Race, Valerie; Peeters, Hilde; Corveleyn, Anniek; Coban‐Akdemir, Zeynep; Jhangiani, Shalini N.; Song, Xiaofei; Mubungu, Gerrye; Posey, Jennifer; Lupski, James R.; Vermeesch, Joris R.; Lukusa, Prosper; Devriendt, Koenraad
Journal:
American journal of medical genetics
Issue:
Volume 176:Issue 9(2018)
Page Start:
1897
Record Type:
Journal Article
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2. A Distinct Class of Chromoanagenesis Events Characterized by Focal Copy Number Gains. Issue 7 (6th April 2016)

Authors:
Masset, Heleen; Hestand, Matthew S.; Van Esch, Hilde; Kleinfinger, Pascale; Plaisancié, Julie; Afenjar, Alexandra; Molignier, Romain; Schluth‐Bolard, Caroline; Sanlaville, Damien; Vermeesch, Joris R.
Journal:
Human mutation
Issue:
Volume 37:Issue 7(2016)
Page Start:
661
Record Type:
Journal Article
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3. Accuracy and Clinical Value of Maternal Incidental Findings During Noninvasive Prenatal Testing for Fetal Aneuploidies. Issue 8 (August 2017)

Authors:
Brison, Nathalie; van den Bogaert, Kris; Dehaspe, Luc; van den Oever, Jessica M. E.; Janssens, Katrien; Blaumeiser, Bettina; Peeters, Hilde; van Esch, Hilde; van Buggenhout, Griet; Vogels, Annick; de Ravel, Thomy; Legius, Eric; Devriendt, Koen; Vermeesch, Joris R.
Journal:
Obstetrical & gynecological survey
Issue:
Volume 72:Issue 8(2017)
Page Start:
Record Type:
Journal Article
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4. Agilent Technologies OnePGT solution: External verification on both blastomere and trophectoderm biopsies. (April 2019)

Authors:
Esteki, Masoud. Zamani; Melotte, Cindy; Coonen, Edith; Dreesen, Joseph; Paulussen, Aimee; Dumoulin, John; Van Uum, Christian; Drusedau, Marion; Engelen, John; Derks, Kasper; Van Golde, R.; Dimitriadou, Eftychia; Masset, Heleen; François, Katrien O.; Allemeersch, Joke; Richards, Rebecca; Moeys, Sa...
Journal:
Reproductive biomedicine online
Issue:
Volume 38(2019)Supplement 1
Page Start:
e11
Record Type:
Journal Article
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7. Diagnostic implications of genetic copy number variation in epilepsy plus. (13th March 2019)

Authors:
Coppola, Antonietta; Cellini, Elena; Stamberger, Hannah; Saarentaus, Elmo; Cetica, Valentina; Lal, Dennis; Djémié, Tania; Bartnik‐Glaska, Magdalena; Ceulemans, Berten; Helen Cross, J.; Deconinck, Tine; Masi, Salvatore De; Dorn, Thomas; Guerrini, Renzo; Hoffman‐Zacharska, Dorotha; Kooy, Frank; Lag...
Other Names:
Lehesjioki Anna‐Elina investigator.; Craiu Dana investigator.; Talvik Tiina investigator.; Caglayan Hande investigator.; Serratosa Jose investigator.; Sterbova Katalin investigator.; Møller Rikke S. investigator.; Hjalgrim Helle investigator.; Lerche Holger investigator.; Weber Yvonne investigato...
Journal:
Epilepsia
Issue:
Volume 60:issue 4(2019)
Page Start:
689
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗