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Chromosomal rearrangements in the 11p15 imprinted region: 17 new 11p15.5 duplications with associated phenotypes and putative functional consequences
Laboratoire de recherches Intégratives en Neurosciences et psychologie Cognitive UR-LINC
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Chromosomal rearrangements in the 11p15 imprinted region: 17 new 11p15.5 duplications with associated phenotypes and putative functional consequences
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Clinical and molecular findings in 39 patients with KBG syndrome caused by deletion or mutation of ANKRD11
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An Application of NGS for Molecular Investigations in Perrault Syndrome: Study of 14 Families and Review of the Literature
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