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The Belgian MicroArray Prenatal (BEMAPRE) database: A systematic nationwide repository of fetal genomic aberrations.
Prenat Diagn. 2018 Dec;38(13):1120-1128. doi: 10.1002/pd.5373. Epub 2018 Nov 14.
Prenat Diagn. 2018.
PMID: 30334587
Prenatally detected copy number variants in a national cohort: A postnatal follow-up study.
Muys J, Jacquemyn Y, Blaumeiser B, Bourlard L, Brison N, Bulk S, Chiarappa P, De Leener A, De Rademaeker M, Désir J, Destrée A, Devriendt K, Dheedene A, Duquenne A, Fieuw A, Fransen E, Gatot JS, Jamar M, Janssens S, Kerstjens J, Keymolen K, Lederer D, Menten B, Pichon B, Rombout S, Sznajer Y, Van Den Bogaert A, Van Den Bogaert K, Vermeesch J, Janssens K.
Muys J, et al. Among authors: rombout s.
Prenat Diagn. 2020 Sep;40(10):1272-1283. doi: 10.1002/pd.5751. Epub 2020 Jun 24.
Prenat Diagn. 2020.
PMID: 32436253
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Implementation of genomic arrays in prenatal diagnosis: the Belgian approach to meet the challenges.
Vanakker O, Vilain C, Janssens K, Van der Aa N, Smits G, Bandelier C, Blaumeiser B, Bulk S, Caberg JH, De Leener A, De Rademaeker M, de Ravel T, Desir J, Destree A, Dheedene A, Gaillez S, Grisart B, Hellin AC, Janssens S, Keymolen K, Menten B, Pichon B, Ravoet M, Revencu N, Rombout S, Staessens C, Van Den Bogaert A, Van Den Bogaert K, Vermeesch JR, Kooy F, Sznajer Y, Devriendt K.
Vanakker O, et al. Among authors: rombout s.
Eur J Med Genet. 2014 Mar;57(4):151-6. doi: 10.1016/j.ejmg.2014.02.002. Epub 2014 Feb 15.
Eur J Med Genet. 2014.
PMID: 24534801
Review.
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A rare case of de novo distal 19q trisomy prenatally diagnosed.
Rombout S, Sartenaer D, Parmentier B, Dugauquier C, Gillerot Y.
Rombout S, et al.
Prenat Diagn. 2004 Oct;24(10):822-7. doi: 10.1002/pd.995.
Prenat Diagn. 2004.
PMID: 15503276
Review.
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Prenatal diagnosis of trisomy 6 mosaicism.
Destree A, Fourneau C, Dugauquier C, Rombout S, Sartenaer D, Gillerot Y.
Destree A, et al. Among authors: rombout s.
Prenat Diagn. 2005 May;25(5):354-7. doi: 10.1002/pd.1149.
Prenat Diagn. 2005.
PMID: 15906424
Review.
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Frequency of Participation in External Quality Assessment Programs Focused on Rare Diseases: Belgian Guidelines for Human Genetics Centers.
Lantoine J, Brysse A, Dideberg V, Claes K, Symoens S, Coucke W, Benoit V, Rombout S, De Rycke M, Seneca S, Van Laer L, Wuyts W, Corveleyn A, Van Den Bogaert K, Rydlewski C, Wilkin F, Ravoet M, Fastré E, Capron A, Vandevelde NM.
Lantoine J, et al. Among authors: rombout s.
JMIR Med Inform. 2021 Jul 12;9(7):e27980. doi: 10.2196/27980.
JMIR Med Inform. 2021.
PMID: 34255700
Free PMC article.
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Pure terminal duplication of the short arm of chromosome 19 in a boy with mild microcephaly.
Andries S, Sartenaer D, Rack K, Rombout S, Tuerlinckx D, Gillerot Y, Van Maldergem L.
Andries S, et al. Among authors: rombout s.
J Med Genet. 2002 Oct;39(10):E60. doi: 10.1136/jmg.39.10.e60.
J Med Genet. 2002.
PMID: 12362042
Free PMC article.
No abstract available.
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Adverse events in apheresis: An update of the WAA registry data.
Mörtzell Henriksson M, Newman E, Witt V, Derfler K, Leitner G, Eloot S, Dhondt A, Deeren D, Rock G, Ptak J, Blaha M, Lanska M, Gasova Z, Hrdlickova R, Ramlow W, Prophet H, Liumbruno G, Mori E, Griskevicius A, Audzijoniene J, Vrielink H, Rombout S, Aandahl A, Sikole A, Tomaz J, Lalic K, Mazic S, Strineholm V, Brink B, Berlin G, Dykes J, Toss F, Axelsson CG, Stegmayr B, Nilsson T, Norda R, Knutson F, Ramsauer B, Wahlström A.
Mörtzell Henriksson M, et al. Among authors: rombout s.
Transfus Apher Sci. 2016 Feb;54(1):2-15. doi: 10.1016/j.transci.2016.01.003. Epub 2016 Jan 8.
Transfus Apher Sci. 2016.
PMID: 26776481
Free article.
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