Molecular cytogenetic characterization and genotype/phenotype analysis in a patient with a de novo 8p23.2p23.3 deletion/12p13.31p13.33 duplication

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作者： Margari,L. ^[1] ; DiCosola,M.L. ^[2] ; Buttiglione,M. ^[3] ; Pansini,A. ^[4] ; Buonadonna,A.L. ; Craig,F. ; Cariola,F. ; Petruzzelli,M.G. ; Gentile,M.

作者单位： Department of Medical Genetics, Hospital Di Venere, ASL BARI, Bari, Italy ^[1] Department of Neurological and Psychiatric Sciences, Child and Adoloscence Neuropsychiatric Unit ^[2] Department of Research, Medical Genetic Unit, IRCCS Saverio de Bellis, Castellana Grotte (BA), ^[3] Department of Research, Medical Genetic Unit, IRCCS Saverio de Bellis, Castellana Grotte (BA), Italy ^[4]

关键词 Array CGH MCA/MR syndrome Monosomy 8p Trisomy 12p

发布时间 2013-11-20

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American journal of medical genetics, Part A

2012年158A卷7期

1713-1718页

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Molecular cytogenetic characterization and genotype/phenotype analysis in a patient with a de novo 8p23.2p23.3 deletion/12p13.31p13.33 duplication

American journal of medical genetics, Part A

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American journal of medical genetics, Part A

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Molecular cytogenetic characterization and genotype/phenotype analysis in a patient with a de novo 8p23.2p23.3 deletion/12p13.31p13.33 duplication

American journal of medical genetics, Part A

相似文献

American journal of medical genetics, Part A

相关期刊

检索历史清除