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Q34328657-4D627B7A-B977-4377-891E-D37ACF0AED2E
Q34328657-4D627B7A-B977-4377-891E-D37ACF0AED2E
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http://www.wikidata.org/entity/statement/Q34328657-4D627B7A-B977-4377-891E-D37ACF0AED2E
Familial interstitial Xq27.3q28 duplication encompassing the FMR1 gene but not the MECP2 gene causes a new syndromic mental retardation condition
P2860
Q34328657-4D627B7A-B977-4377-891E-D37ACF0AED2E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34328657-4D627B7A-B977-4377-891E-D37ACF0AED2E
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wasDerivedFrom
d0ad702d8aa93f80ea130ce9837baf346b2efbd8
P2860
The clinical picture of the Börjeson-Forssman-Lehmann syndrome in males and heterozygous females with PHF6 mutations.