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EN19p13.3 Microduplication Syndrome
Alias:
Dup(19)(p13.13)
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19p13.3 Microduplication Syndrome, also known as dup(19)(p13.13), is related to tietz albinism-deafness syndrome and microcephaly. An important gene associated with 19p13.3 Microduplication Syndrome is NFIX (Nuclear Factor I X). Related phenotypes are global developmental delay and delayed speech and language development
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MALACARDS
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