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Smith–Fineman–Myers syndrome (SFMS1) is a congenital disorder that causes birth defects. This syndrome was named after Richard D. Smith, Robert M. Fineman and Gart G. Myers who discovered it around 1980.

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dbo:abstract
  • Smith–Fineman–Myers syndrome (SFMS1) is a congenital disorder that causes birth defects. This syndrome was named after Richard D. Smith, Robert M. Fineman and Gart G. Myers who discovered it around 1980. (en)
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  • C537445
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  • Smith–Fineman–Myers syndrome has an X-linked recessive pattern of inheritance. (en)
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  • Smith–Fineman–Myers syndrome (en)
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  • 719212004 (xsd:integer)
dbp:synonyms
  • X-linked mental retardation-hypotonic facies syndrome 1 , Carpenter–Waziri syndrome, Chudley–Lowry syndrome, SFMS, Holmes–Gang syndrome and Juberg–Marsidi syndrome , (en)
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rdfs:comment
  • Smith–Fineman–Myers syndrome (SFMS1) is a congenital disorder that causes birth defects. This syndrome was named after Richard D. Smith, Robert M. Fineman and Gart G. Myers who discovered it around 1980. (en)
rdfs:label
  • Smith–Fineman–Myers-Syndrom (de)
  • Smith–Fineman–Myers syndrome (en)
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  • Smith–Fineman–Myers syndrome (en)
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