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Search Results - Magielsen, Frank J
Search Results - Magielsen, Frank J
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Genome-wide methylation analysis in patients with proximal hypospadias - a pilot study and review of the literature
by
van Bever, Yolande
,
Boers, Ruben G
,
Brüggenwirth, Hennie T
,
van IJcken, Wilfred Fj
,
Magielsen, Frank J
,
de Klein, Annelies
,
Boers, Joachim B
,
Looijenga, Leendert Hj
,
Brosens, Erwin
,
Gribnau, Joost
,
Hannema, Sabine E
Published in
Epigenetics
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Identification of Early-Onset Metastasis in SF3B1 Mutated Uveal Melanoma
by
Drabarek, Wojtek
,
van Riet, Job
,
Nguyen, Josephine Q N
,
Smit, Kyra N
,
van Poppelen, Natasha M
,
Jansen, Rick
,
Medico-Salsench, Eva
,
Vaarwater, Jolanda
,
Magielsen, Frank J
,
Brands, Tom
,
Eussen, Bert
,
Bosch, Thierry P P van den
,
Verdijk, Robert M
,
Naus, Nicole C
,
Paridaens, Dion
,
de Klein, Annelies
,
Brosens, Erwin
,
van de Werken, Harmen J G
,
Kilic, Emine
,
On Behalf Of The Rotterdam Ocular Melanoma Study Group
Published in
Cancers
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Identification of Rare Variants Involved in High Myopia Unraveled by Whole Genome Sequencing
by
Haarman, Annechien E.G.
,
Klaver, Caroline C.W.
,
Tedja, Milly S.
,
Roosing, Susanne
,
Astuti, Galuh
,
Gilissen, Christian
,
Hoefsloot, Lies H.
,
van Tienhoven, Marianne
,
Brands, Tom
,
Magielsen, Frank J.
,
Eussen, Bert H.J.F.M.M.
,
de Klein, Annelies
,
Brosens, Erwin
,
Verhoeven, Virginie J.M.
Published in
Ophthalmology science (Online)
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Identification of Intragenic Exon Deletions and Duplication of TCF12 by Whole Genome or Targeted Sequencing as a Cause of TCF12-Related Craniosynostosis
by
Goos, Jacqueline A.C.
,
Fenwick, Aimee L.
,
Swagemakers, Sigrid M.A.
,
McGowan, Simon J.
,
Knight, Samantha J.L.
,
Twigg, Stephen R.F.
,
Hoogeboom, A. Jeannette M.
,
van Dooren, Marieke F.
,
Magielsen, Frank J.
,
Wall, Steven A.
,
Mathijssen, Irene M.J.
,
Wilkie, Andrew O.M.
,
van der Spek, Peter J.
,
van den Ouweland, Ans M.W.
Published in
Human mutation
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Identification of causative variants in TXNL4A in Burn-McKeown syndrome and isolated choanal atresia
by
Goos, Jacqueline A C
,
Swagemakers, Sigrid M A
,
Twigg, Stephen R F
,
van Dooren, Marieke F
,
Hoogeboom, A Jeannette M
,
Beetz, Christian
,
Günther, Sven
,
Magielsen, Frank J
,
Ockeloen, Charlotte W
,
A Ramos-Arroyo, Maria
,
Pfundt, Rolph
,
Yntema, Helger G
,
van der Spek, Peter J
,
Stanier, Philip
,
Wieczorek, Dagmar
,
Wilkie, Andrew O M
,
van den Ouweland, Ans M W
,
Mathijssen, Irene M J
,
Hurst, Jane A
Published in
European journal of human genetics : EJHG
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Fast detection of FOXF1 variants in patients with alveolar capillary dysplasia with misalignment of pulmonary veins using targeted sequencing
by
Slot, Evelien
,
von der Thüsen, Jan H
,
van Heijst, Arno
,
van Marion, Ronald
,
Magielsen, Frank
,
Dubbink, Hendrikus J
,
Post, Martin
,
Debeer, Anne
,
Tibboel, Dick
,
Rottier, Robbert J
,
de Klein, Annelies
Published in
Pediatric research
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Molecular Genetics of Conjunctival Melanoma and Prognostic Value of TERT Promoter Mutation Analysis
by
van Poppelen, Natasha M.
,
van Ipenburg, Jolique A.
,
van den Bosch, Quincy
,
Vaarwater, Jolanda
,
Brands, Tom
,
Eussen, Bert
,
Magielsen, Frank
,
Dubbink, Hendrikus J.
,
Paridaens, Dion
,
Brosens, Erwin
,
Naus, Nicole
,
de Klein, Annelies
,
Kiliç, Emine
,
Verdijk, Robert M.
Published in
International journal of molecular sciences
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Case Report and Review of the Literature: Congenital Diaphragmatic Hernia and Craniosynostosis, a Coincidence or Common Cause?
by
Gaillard, Linda
,
Goverde, Anne
,
van den Bosch, Quincy C C
,
Jehee, Fernanda S
,
Brosens, Erwin
,
Veenma, Danielle
,
Magielsen, Frank
,
de Klein, Annelies
,
Mathijssen, Irene M J
,
van Dooren, Marieke F
Published in
Frontiers in pediatrics
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Case Report and Review of the Literature: Congenital Diaphragmatic Hernia and Craniosynostosis, a Coincidence or Common Cause?
by
Gaillard, Linda
,
Goverde, Anne
,
van den Bosch, Quincy C C
,
Jehee, Fernanda S
,
Brosens, Erwin
,
Veenma, Danielle
,
Magielsen, Frank
,
de Klein, Annelies
,
Mathijssen, Irene M J
,
van Dooren, Marieke F
Published in
Frontiers in pediatrics
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