No abstract available
MeSH terms
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Abnormalities, Multiple / genetics
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Casein Kinase II / genetics*
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Casein Kinase II / metabolism
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Child, Preschool
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Chromosome Deletion*
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Chromosomes, Human, Pair 6 / genetics*
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Craniofacial Abnormalities / genetics
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Gene Deletion
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Humans
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Intellectual Disability / genetics
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Male
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Megalencephaly / genetics
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Musculoskeletal Abnormalities / genetics
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Phenotype
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Syndrome