13q Deletion and central nervous system anomalies: further insights from karyotype–phenotype analyses of 14 patients

BACKGROUND: Chromosome 13q deletion is associated with varying phenotypes, which seem to depend on the location of the deleted segment. Although various attempts have been made to link the 13q deletion intervals to distinct phenotypes, there is still no acknowledged consensus correlation between the...

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Detalles Bibliográficos
Main Authors: Ballarati, Lucia, Rossi, Elena, Bonati, Maria Teresa, Gimelli, Stefania, Maraschio, Paola, Finelli, Palma, Giglio, Sabrina, Lapi, Elisabetta, Bedeschi, Maria Francesca, Guerneri, Silvana, Arrigo, Giulia, Patricelli, Maria Grazia, Mattina, Teresa, Guzzardi, Oriana, Pecile, Vanna, Police, Adalgisa, Scarano, Gioacchino, Larizza, Lidia, Zuffardi, Orsetta, Giardino, Daniela
Formato: Artigo
Idioma:Inglês
Publicado: BMJ Group 2007
Assuntos:
Electronic Letter
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC2597907/
https://ncbi.nlm.nih.gov/pubmed/17209130
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.2006.043059
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