Prenatal diagnosis of Wolf-Hirschhorn syndrome confirmed by comparative genomic hybridization array: report of two cases and review of the literature

Wolf-Hirschhorn syndrome (WHS) is a well known genetic condition caused by a partial deletion of the short arm of chromosome 4. The great variability in the extent of the 4p deletion and the possible contribution of additional genetic rearrangements lead to a wide spectrum of clinical manifestations...

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Detalhes bibliográficos
Main Authors: Sifakis, Stavros, Manolakos, Emmanouil, Vetro, Annalisa, Kappou, Dimitra, Peitsidis, Panagiotis, Kontodiou, Maria, Garas, Antonios, Vrachnis, Nikolaos, Konstandinidou, Anastasia, Zuffardi, Orsetta, Orru, Sandro, Papoulidis, Ioannis
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2012
Assuntos:
Case Report
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3307480/
https://ncbi.nlm.nih.gov/pubmed/22373435
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1755-8166-5-12
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