Molecular characterization of an analphoid supernumerary marker chromosome derived from 18q22.1➔qter in prenatal diagnosis: a case report

BACKGROUND: Small supernumerary marker chromosomes (sSMC) occur in 0.072% of unselected cases of prenatal diagnoses, and their molecular cytogenetic characterization is required to establish a reliable karyotype-phenotype correlation. A small group of sSMC are C-band-negative and devoid of alpha-sat...

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Detalles Bibliográficos
Autores principales: Altieri, Vincenzo, Capozzi, Oronzo, Marzano, Maria Cristina, Catapano, Oriana, Di Biase, Immacolata, Rocchi, Mariano, De Tollis, Giuliana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4213471/
https://www.ncbi.nlm.nih.gov/pubmed/25360155
http://dx.doi.org/10.1186/s13039-014-0069-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4213471/
https://www.ncbi.nlm.nih.gov/pubmed/25360155
http://dx.doi.org/10.1186/s13039-014-0069-4

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