Prenatal diagnosis of severe structural congenital malformations in Europe
Garne, E., Loane, M., Dolk, H., De Vigan, C., Scarano, G., Tucker, D., Stoll, C., Gener, B., Pierini, A., Nelen, V., Rösch, C., Gillerot, Y., Feijoo, M., Tincheva, R., Queisser‐Luft, A., Addor, M.‐C., Mosquera, C., Gatt, M., Barisic, I.
Published in Ultrasound in obstetrics & gynecology (01.01.2005)
Published in Ultrasound in obstetrics & gynecology (01.01.2005)
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Mutations in FKBP10 cause recessive osteogenesis imperfecta and bruck syndrome
Kelley, B. P, Malfait, F, Bonafe, L, Baldridge, D, Homan, E, Symoens, S, Willaert, A, Elcioglu, N, Van Maldergem, Lionel, Verellen-Dumoulin, C, Gillerot, Y, Napierala, D, Krakow, D, Beighton, P, Superti-Furga, A, De Paepe, Alexandra, Lee, B
Published in Journal of bone and mineral research (01.03.2011)
Published in Journal of bone and mineral research (01.03.2011)
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Revisiting the craniosynostosis-radial ray hypoplasia association: Baller-Gerold syndrome caused by mutations in the RECQL4 gene
Van Maldergem, L, Siitonen, H A, Jalkh, N, Chouery, E, De Roy, M, Delague, V, Muenke, M, Jabs, E W, Cai, J, Wang, L L, Plon, S E, Fourneau, C, Kestilä, M, Gillerot, Y, Mégarbané, A, Verloes, A
Published in Journal of medical genetics (01.02.2006)
Published in Journal of medical genetics (01.02.2006)
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Partial NSD1 deletions cause 5% of Sotos syndrome and are readily identifiable by multiplex ligation dependent probe amplification
Douglas, J, Tatton-Brown, K, Coleman, K, Guerrero, S, Berg, J, Cole, T R P, FitzPatrick, D, Gillerot, Y, Hughes, H E, Pilz, D, Raymond, F L, Temple, I K, Irrthum, A, Schouten, J P, Rahman, N
Published in Journal of medical genetics (01.09.2005)
Published in Journal of medical genetics (01.09.2005)
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IRF6 Screening of Syndromic and a priori Non-Syndromic Cleft Lip and Palate Patients: Identification of a New Type of Minor VWS Sign
Desmyter, L, Ghassibe, M, Revencu, N, Boute, O, Lees, M, Francois, G, Verellen-Dumoulin, C, Sznajer, Y, Moncla, A, Benateau, H, Claes, K, Devriendt, K, Mathieu, M, Van Maldergem, Lionel, Addor, M. C, Drouin-Garraud, V, Mortier, G, Bouma, M, Dieux-Coeslier, A, Genevieve, D, Goldenberg, A, Gozu, A, Makrythanasis, P, McEntagart, U, Sanchez, A, Vilain, C, Vermeer, S, Connell, F, Verheij, J, Manouvrier, S, Pierquin, Geneviève, Odent, S, Holder-Espinasse, M, Vincent-Delorme, C, Gillerot, Y, Vanwijck, R, Bayet, B, Vikkula, M
Published in Molecular syndromology (01.01.2010)
Published in Molecular syndromology (01.01.2010)
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Translocation of BCL2 and BCL6 to the same immunoglobulin heavy chain locus in a case of Follicular Lymphoma
Rack, K., Delannoy, A., Ravoet, C., Vannuffel, P., Hamels, J., Gillerot, Y.
Published in Leukemia & lymphoma (01.10.2005)
Published in Leukemia & lymphoma (01.10.2005)
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Prenatal diagnosis of trisomy 6 mosaicism
Destree, A., Fourneau, C., Dugauquier, C., Rombout, S., Sartenaer, D., Gillerot, Y.
Published in Prenatal diagnosis (01.05.2005)
Published in Prenatal diagnosis (01.05.2005)
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Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation
Limaye, Nisha, Revencu, N, Van Regemorter, N, Garzon, M, Bonduelle, M, Chung, W, Daras, M D, Fahey, M C, Garrett, C, Gillerot, Y, Gillessen-Kaesbach, G, Giménez-Arnau, A, Guzzetta, F, Battaglia, D, Heimdal, K, Lissens, W, Taub, E, Van Maldergem, L, Van Paesschen, W, Wieczorek, D, Wood, N W, Boon, L, Vikkula, M
Published in Human genetics (01.12.2007)
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Published in Human genetics (01.12.2007)
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Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation
Limaye, Nisha, Revencu, N, Van Regemorter, N, Garzon, M, Bonduelle, M, Chung, W, Daras, M D, Fahey, M C, Garrett, C, Gillerot, Y, Gillessen-Kaesbach, G, Giménez-Arnau, A, Guzzetta, F, Battaglia, D, Heimda, K, Lissens, W, Taub, E, Van Maldergem, L, Van Paesschen, W, Wieczorek, D, Wood, N W, Boon, L, Vikkula, M
Published in Human genetics (01.12.2007)
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Published in Human genetics (01.12.2007)
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Prenatal diagnostic procedures used in pregnancies with congenital malformations in 14 regions of Europe
Garne, Ester, Loane, Maria, de Vigan, Catherine, Scarano, Gioacchino, de Walle, Hermien, Gillerot, Yves, Stoll, Claude, Addor, Marie-Claude, Stone, David, Gener, Blanca, Feijoo, Maria, Mosquera-Tenreiro, Carmen, Gatt, Miriam, Queisser-Luft, Annette, Baena, Neus, Dolk, Helen
Published in Prenatal diagnosis (01.11.2004)
Published in Prenatal diagnosis (01.11.2004)
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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
Published in Journal of medical genetics (01.10.2002)
Published in Journal of medical genetics (01.10.2002)
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Major Decrease in the Incidence of Trisomy 21 at Birth in South Belgium: Mass Impact of Triple Test?
Verloes, Alain, Gillerot, Y, Van Maldergem, Lionel, Schoos, Roland, Herens, Christian, Jamar, Michelle, Dideberg, Vinciane, Lesenfants, S, Koulischer, Lucien
Published in European journal of human genetics : EJHG (2001)
Published in European journal of human genetics : EJHG (2001)
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Gene symbol: IRF6. Disease: Van der Woude syndrome
Ghassibe, M, Revencu, N, Bayet, B, Gillerot, Y, Vanwijck, R, Verellen-Dumoulin, C, Vikkula, M
Published in Human genetics (01.11.2003)
Published in Human genetics (01.11.2003)
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Gene symbol: IRF6. Disease: Van der Woude syndrome
Ghassibe, M, Revencu, N, Bayet, B, Gillerot, Y, Vanwijck, R, Verellen-Dumoulin, C, Vikkula, M
Published in Human genetics (01.11.2003)
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Published in Human genetics (01.11.2003)
Journal Article
Gene symbol: IRF6. Disease: Van der Woude syndrome
Ghassibe, M, Revencu, N, Bayet, B, Gillerot, Y, Vanwijck, R, Verellen-Dumoulin, C, Vikkula, M
Published in Human genetics (01.11.2003)
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Published in Human genetics (01.11.2003)
Journal Article
Orofacial clefting: update on the role of genetics
Ghassibe, M, Bayet, B, Revencu, N, Desmyter, L, Verellen-Dumoulin, C, Gillerot, Y, Deggouj, N, Vanwijck, R, Vikkula, M
Published in B-ENT (Leuven) (2006)
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Published in B-ENT (Leuven) (2006)
Journal Article
Lethal femoral-facial syndrome: a case with unusual manifestations
Gillerot, Y, Fourneau, C, Willems, T, Van Maldergem, L
Published in Journal of medical genetics (01.06.1997)
Published in Journal of medical genetics (01.06.1997)
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Anaesthetic management of a child with Marshall-Smith syndrome
DERNEDDE, G, PENDEVILLE, P, VEYCKEMANS, F, VERELLEN, G, GILLEROT, Y
Published in Canadian journal of anesthesia (01.07.1998)
Published in Canadian journal of anesthesia (01.07.1998)
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Two cases of maternal antenatal splenic rupture and hypotension associated with moebius syndrome and cerebral palsy in offspring : Further evidence for a utero placental vascular aetiology for the Moebius syndrome and some cases of cerebral palsy
LIPSON, A. H, GILLEROT, Y, TANNENBERG, A. E. G, GIURGEA, S
Published in European journal of pediatrics (01.09.1996)
Published in European journal of pediatrics (01.09.1996)
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