Rare – Page 338 – CheckOrphan

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Benign familial infantile epilepsy

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Chromosome 13q trisomy

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Chromosome 13q deletion

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Chromosome 14- trisomy mosaic

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Ring chromosome 14 syndrome

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Chromosome 13p duplication

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Chromosome 13- partial monosomy 13q

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Craniofacial deafness hand syndrome

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Chromosome 14 deletion

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Chromosome 13q-mosaicism

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