Cytogenetic and Array-CGH Characterization of a Complex de novo Rearrangement Involving Duplication and Deletion of 9p and Clinical Findings in a 4-Month-Old Female

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Cytogenetic and Genome Research, Vol. 126, Iss. 3, 2010-01 ,pp. : 305-312

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Another Rare Case of a Child with de novo Terminal 9p Deletion and Co-Existing Interstitial 9p Duplication: Clinical Findings and Molecular Cytogenetic Study by Array-CGH

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Cytogenetic and Genome Research, Vol. 139, Iss. 1, 2012-09 ,pp. : 9-16

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Detection of a novel familial deletion of four genes between BP1 and BP2 of the Prader-Willi/Angelman syndrome critical region by oligo-array CGH in a child with neurological disorder and speech impairment

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Cytogenetic and Genome Research, Vol. 116, Iss. 1-2, 2007-02 ,pp. : 135-140

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Whole-genome array-CGH for detection of submicroscopic chromosomal imbalances in children with mental retardation

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Cytogenetic and Genome Research, Vol. 118, Iss. 1, 2007-09 ,pp. : 1-7

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Pre- and Postnatal Diagnosis of 10p14 Deletion and 22q11.2 Deletion Syndrome and Significance of Non-Cardiac Markers

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Cytogenetic and Genome Research, Vol. 148, Iss. 4, 2016-06 ,pp. : 249-255

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