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British Medical Bulletin|June 23, 2023
Placing joint hypermobility in context: traits, disorders and syndromesSilvia Morlino, Marco CastoriAmerican Journal of Medical Genetics. Part C, Seminars in Medical Genetics|March 31, 2015
Gastrointestinal and nutritional issues in joint hypermobility syndrome/Ehlers-Danlos syndrome, hypermobility typeMarco Castori, Silvia Morlino, Giulia Pascolini, et al.Genes|June 13, 2019
Characterization of Two Novel Intronic Variants Affecting <i>Splicing</i> in <i>FBN1</i>-Related DisordersCarmela Fusco, Silvia Morlino, Lucia Micale, et al.Birth Defects Research. Part A, Clinical and Molecular Teratology|November 1, 2014
Oropharyngeal teratoma, oral duplication, cervical diplomyelia and anencephaly in a 22-week fetus: A review of the craniofacial teratoma syndromeSilvia Morlino, Marco Castori, Francesca Servadei, et al.Rheumatology (Oxford, England)|February 21, 2019
Severity classes in adults with hypermobile Ehlers-Danlos syndrome/hypermobility spectrum disorders: a pilot study of 105 Italian patientsMassimiliano Copetti, Silvia Morlino, Marina Colombi, et al.Journal of Child Neurology|July 20, 2014
An additional patient with 3q27.3 microdeletion syndromeMarco Castori, Irene Bottillo, Luigi Laino, et al.American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|February 7, 2015
Connective tissue, Ehlers-Danlos syndrome(s), and head and cervical painMarco Castori, Silvia Morlino, Giulia Ghibellini, et al.American Journal of Medical Genetics. Part A|March 2, 2019
Cardiac valvular Ehlers-Danlos syndrome is a well-defined condition due to recessive null variants in COL1A2Vito Guarnieri, Silvia Morlino, Giuseppe Di Stolfo, et al.American Journal of Medical Genetics. Part A|December 28, 2020
Review of clinical and molecular variability in autosomal recessive cutis laxa 2ASilvia Morlino, Grazia Nardella, Stefano Castellana, et al.Birth Defects Research. Part A, Clinical and Molecular Teratology|December 15, 2015
Variability in a three-generation family with Pierre Robin sequence, acampomelic campomelic dysplasia, and intellectual disability due to a novel ∼1 Mb deletion upstream of SOX9, and including KCNJ2 and KCNJ16Marco Castori, Irene Bottillo, Silvia Morlino, et al.Pageof 6