Prenatal diagnosis of two de novo 4q35-qter deletions characterized by array-CGH

BACKGROUND: The 4q- syndrome is a well known genetic condition caused by a partial terminal or interstitial deletion in the long arm of chromosome 4. The great variability in the extent of these deletions and the possible contribution of additional genetic rearrangements, such as unbalanced transloc...

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Détails bibliographiques
Auteurs principaux: Manolakos, Emmanouil, Kefalas, Konstantinos, Vetro, Annalisa, Oikonomidou, Eirini, Daskalakis, George, Psara, Natasa, Siomou, Elisa, Papageorgiou, Elena, Sevastopoulou, Eirini, Konstantinidou, Anastasia, Vrachnis, Nikolaos, Thomaidis, Loretta, Zuffardi, Orsetta, Papoulidis, Ioannis
Format: Artigo
Langue:Inglês
Publié: BioMed Central 2013
Sujets:
Research
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC3843522/
https://ncbi.nlm.nih.gov/pubmed/24176130
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1755-8166-6-47
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