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American Journal of Medical Genetics|March 29, 2002
Kallmann syndrome in a patient with congenital spherocytosis and an interstitial 8p11.2 deletionStefan Vermeulen, Ludwine Messiaen, Petra Scheir, et al.Community Genetics|February 5, 2005
Marfan syndrome in EuropeSylvia De Bie, Anne De Paepe, Isabelle Delvaux, et al.European Journal of Human Genetics : EJHG|September 5, 2013
Occipital horn syndrome and classical Menkes Syndrome caused by deep intronic mutations, leading to the activation of ATP7A pseudo-exonSaiqa Yasmeen, Katrine Lund, Anne De Paepe, et al.Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|April 1, 2005
Unequivocal delineation of clinicogenetic subgroups and development of a new model for improved outcome prediction in neuroblastomaJo Vandesompele, Michael Baudis, Katleen De Preter, et al.Pageof 1