H3 histone family member 3B
OMIM: 601058, Gene2Phenotype
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H3F3B in Rare syndromic craniosynostosis or isolated multisuture synostosis
Level 3: Craniosynostosis syndromes
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review | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown |
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H3F3B in DDG2P
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review | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown |
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H3F3B in Early onset or syndromic epilepsy
Level 3: Inherited Epilepsy Syndromes
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review | MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted |
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H3F3B in Intellectual disability - microarray and sequencing
Level 3: Neurodevelopmental disorders
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review | MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted |
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