No abstract available
MeSH terms
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Abnormalities, Multiple / diagnosis*
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Abnormalities, Multiple / genetics
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COUP Transcription Factor I / genetics*
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Child
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Chromosome Deletion
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Chromosomes, Human, Pair 5
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Developmental Disabilities / diagnosis*
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Developmental Disabilities / genetics
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Haploinsufficiency*
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Humans
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Molecular Diagnostic Techniques
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Oligonucleotide Array Sequence Analysis
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Optic Atrophy / diagnosis*
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Optic Atrophy / genetics
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Polymorphism, Single Nucleotide
Substances
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COUP Transcription Factor I
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NR2F1 protein, human