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All Publications

Displaying 11 results.
    • Journal article
    Deletion and Point Mutations of PTHLH Cause Brachydactyly Type E
    Klopocki, Eva Hennig, Bianca P. Dathe, Katarina Koll, Randi de Ravel, Thomy Baten, Emiel Blom, Eveline Gillerot, Yves[UCL] Weigel, Johannes F. W. Krueger, Gabriele Hiort, Olaf Seemann, Petra Mundlos, Stefan (2010) American Journal of Human Genetics — Vol. 86, no. 3, p. 434-9 (2010)
    • Journal article
    External birth defects in southern Vietnam: a population-based study at the grassroots level of health care in Binh Thuan province.
    Hoang, Truong Nguyen, Dung The Nguyen , Phuong Van Ngoc[UCL] Tran, Dong A Gillerot, Yves[UCL] Reding, Raymond[UCL] Robert, Annie[UCL] (2013) BMC Pediatrics — Vol. 13, p. 67 (2013)
    • Journal article
    Mutations in FKBP10 cause recessive osteogenesis imperfecta and bruck syndrome
    Kelley, Brian P. Malfait, Fransiska Bonafe, Luisa Baldridge, Dustin Homan, Erica Symoens, Sofie Willaert, Andy Elcioglu, Nursel Van Maldergem, Lionel Verellen-Dumoulin, Christine[UCL] Gillerot, Yves[UCL] Napierala, Dobrawa Krakow, Deborah Beighton, Peter Superti-Furga, Andrea De Paepe, Anne Lee, Brendan (2011) Journal of Bone and Mineral Research — Vol. 26, no. 3, p. 666-672 (2011)
    • Journal article
    Partial proximal 10q trisomy: a new case associated with biliary atresia
    Lysy, Philippe[UCL] Sibille, Catherine[UCL] Gillerot, Yves[UCL] Smets, Françoise[UCL] Sokal, Etienne[UCL] (2007) Hereditas — Vol. 144, no. 5, p. 191-194 (2007)
    • Journal article
    Cognitive epilepsy: ADHD related to focal EEG discharges.
    Laporte, Nicole[UCL] Sébire, Guillaume[UCL] Gillerot, Yves[UCL] Guerrini, Renzo Ghariani, Sophie[UCL] (2002) Pediatric neurology — Vol. 27, no. 4, p. 307-311 (2002)
    • Dissertation
    Prévention des troubles majeurs du développement : proposition d'une stratégie basée sur la mise au point personnelle de 420 observations
    Gillerot, Yves[UCL] (1994)
    • Journal article
    Isolated bilateral transverse agenesis of the distal segments of the lower limbs at the level of the knee joint in a human fetus.
    Christiaens, Antoine[UCL] Deprez, Pierre[UCL] Amyere, Mustapha[UCL] Mendola, Antonella[UCL] Bernard, Pierre[UCL] Gillerot, Yves[UCL] Clapuyt, Philippe[UCL] Godfraind, Catherine[UCL] Lengelé, Benoît[UCL] Vikkula, Miikka[UCL] Behets Wydemans, Catherine[UCL] (2016) American Journal of Medical Genetics. Part A — Vol. 170, no. 2, p. 523-530 (2016)
    • Journal article
    Interferon regulatory factor-6: a gene predisposing to isolated cleft lip with or without cleft palate in the Belgian population.
    Ghassibé, Michella[UCL] Bayet, Benedicte Revencu, Nicole Dumoulin, Christine[UCL] Gillerot, Yves Vanwijck, Romain[UCL] Vikkula, Miikka[UCL] (2005) European journal of human genetics : EJHG — Vol. 13, no. 11, p. 1239-42 (2005)
    • Journal article
    Six families with van der Woude and/or popliteal pterygium syndrome: all with a mutation in the IRF6 gene.
    Ghassibé, Michella[UCL] Revencu, Nicole[UCL] Bayet, Bénédicte[UCL] Gillerot, Yves[UCL] Vanwijck, Romain[UCL] Dumoulin, Christine[UCL] Vikkula, Miikka[UCL] (2004) Journal of Medical Genetics — Vol. 41, no. 2, p. 1-5 (2004)
    • Journal article
    Orofacial clefting: update on the role of genetics.
    Ghassibé, Michella[UCL] Bayet, Bénédicte[UCL] Revencu, Nicole[UCL] Desmyter, Laurence[UCL] Dumoulin, Christine[UCL] Gillerot, Yves[UCL] Deggouj, Naima[UCL] Vanwijck, Romain[UCL] Vikkula, Miikka[UCL] (2006) B-ENT — Vol. 2 Suppl 4, p. 20-4 (2006)
    • Journal article
    Sporadic In Utero Generalized Edema Caused by Mutations in the Lymphangiogenic Genes VEGFR3 and FOXC2.
    Ghalamkarpour, Arash Debauche, Christian[UCL] Haan, Eric Van Regemorter, Nicole Sznajer, Yves Thomas, Dominique Revencu, Nicole Gillerot, Yves Boon, Laurence M.[UCL] Vikkula, Miikka[UCL] (2009) The Journal of pediatrics — Vol. 155, no. 1, p. 90-3 (2009)