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Q53414942-4BCDDAEE-FD33-4632-9A52-351E3525CB31
Q53414942-4BCDDAEE-FD33-4632-9A52-351E3525CB31
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Statement
http://www.wikidata.org/entity/statement/Q53414942-4BCDDAEE-FD33-4632-9A52-351E3525CB31
A novel chromosome 19p13.12 deletion in a child with multiple congenital anomalies.
P2860
Q53414942-4BCDDAEE-FD33-4632-9A52-351E3525CB31
BestRank
Statement
http://www.wikidata.org/entity/statement/Q53414942-4BCDDAEE-FD33-4632-9A52-351E3525CB31
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wasDerivedFrom
3e7806c7ddf9bd7d96d578a3a601dd9cc298c65a
P2860
Chromosomal microarray analysis (CMA) detects a large X chromosome deletion including FMR1, FMR2, and IDS in a female patient with mental retardation.