No abstract available
Publication types
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Case Reports
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Comment
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Letter
MeSH terms
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Child
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Chromosome Deletion
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Chromosomes, Human, Pair 2*
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Craniofacial Abnormalities*
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Ear, Inner / abnormalities*
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Ear, Middle / abnormalities*
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Female
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Hearing Loss / genetics
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Heart Defects, Congenital*
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Humans
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Syndrome