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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Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3843522/
https://www.ncbi.nlm.nih.gov/pubmed/24176130
http://dx.doi.org/10.1186/1755-8166-6-47

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3843522/
https://www.ncbi.nlm.nih.gov/pubmed/24176130
http://dx.doi.org/10.1186/1755-8166-6-47

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