A non-syndromic intellectual disability associated with a de novo microdeletion at 7q and 18p, microduplication at Xp, and 18q partial trisomy detected using chromosomal microarray analysis approach

BACKGROUNDChromosome abnormalities that segregate with a disease phenotype can facilitate the identification of disease loci and genes. The relationship between chromosome 18 anomalies with severe intellectual disability has attracted the attention of cytogeneticists worldwide. Duplications of the X...

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Veröffentlicht in:	Molecular cytogenetics 2014, Vol.7, p.44-44
Hauptverfasser:	Pinto, Irene Plaza, Minasi, Lysa Bernardes, da Cruz, Alex Silva, de Melo, Aldaires Vieira, da Cruz E Cunha, Damiana Míriam, Pereira, Rodrigo Roncato, Ribeiro, Cristiano Luiz, da Silva, Claudio Carlos, de Melo E Silva, Daniela, da Cruz, Aparecido Divino
Format:	Report
Sprache:	eng
Online-Zugang:	Volltext
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